No
|
What
is….? |
Answer…
|
1
|
Abfraction
|
A regressive
alteration of tooth structure usually involving hard tissue of the permanent dentition leading to loss of tooth surface at the cervical areas of teeth caused by tensile and compressive forces during tooth flexure. Alternatively, Cervical erosive lesions that cannot be attributed to any particular etiology |
2
|
Abrasion
|
A regressive alteration of
tooth structure usually involving hard tissue of the permanent dentition leading to abnormal loss of tooth structure due to non-masticatory physical friction. |
3
|
Abscess
|
A localized
accumulation of pus caused by an infection. Example periapical abscess. |
4
|
Acantholysis
|
A histopathological feature,
characterized by loss of the intercellular bridges of the prickle cell layer (spinous) of the epithelium usually caused by accumulation of fluid or edema in between the keratinocytes. |
5
|
Acanthosis
|
A
histopathological feature, characterized by excessive thickening of the intermediate cell layer or the stratum spinosum resulting in broadening and elongation of the rete pegs. It is considered as one of hall mark of epithelial dysplasia. |
6
|
Acanthosis nigricans
|
A rare acquired dermatological
disease with an abnormal Keratinization process leading to development of velvety brownish alteration of skin. Sometimes this disease may be a marker of malignancy. |
7
|
Accessory cusps
|
A
developmental anomaly of shape characterized extra cusp like the cusp of Caraebilli in maxillary first molar. |
8
|
Acidogenic theory
|
It states that dental caries
is a chemico-parasitic process consisting of two stages- the decalcification of enamel as a preliminary stage followed by dissolution of the softened residue. The acid required for decalcification is synthesized by the fermentation of starch and food residue by the bacteria’s. This theory was proposed by Miller. |
9
|
Acinic cell adenocarcinoma
|
A malignant
salivary gland malignancy that salivary gland cells showing serous acinar differentiation, most commonly found in the parotid gland. |
10
|
Acquired disturbances
|
Disturbances in the structure
or morphology of any organ form birth or during growth and can occur as a result of environmental or hereditary factors. |
11
|
Acquired Immuno Deficiency Syndrome
|
A syndrome
caused by the infection of Human Immunodeficiency Virus causing the suppression of the immune system and predisposing the individual to infections. |
12
|
Acral lentiginous melanoma
|
A melanoma that is a brown in
color irregularly shaped macular lesion that undergoes progression to nodular melanoma. |
13
|
Acrodynia
|
A chronic
mercury exposure in infants and children where it produces a cold clammy skin, erythematous rashes, excessive salivation, and gingivitis may be the features of the condition. |
14
|
Acromegaly
|
A hormonal disorder that
results when the pituitary gland produces excess growth hormone. |
15
|
Actinic chelitis
|
A chronic
inflammatory lesion caused by chronic exposure to actinic or sunlight manifesting in skin of the middle and lower third of face and commonly in lower lips. |
16
|
Actinic keratosis
|
Is a common cutaneous
premalignant lesion caused by exposure to ultraviolet radiation exposure with microscopic changes in epithelium and connective tissues. |
17
|
Actinic lentigo
|
Is a benign,
multiple, freckle like lesion resulting from chronic exposure to ultraviolet damage to skin. |
18
|
Actinomycosis
|
Is an infection of
filamentous, branching, gram positive anaerobic bacteria belonging to actinomycetes family. The supparative reaction is with yellowish sulphur like flecks that are the colonies of the organisms. |
19
|
Acute
|
Of shorter
duration. Usually have severe symptoms. |
20
|
Acute necrotizing ulcerative gingivitis (ANUG)
|
An infection of the gingiva
caused by fusobacterium and Borecellia vincentii affecting inter- dental papillae as a punched out lesion covered by a pseudomembrane. |
21
|
Acute osteomyelitis
|
A rapidly
destructive inflammatory process of bone and soft tissues associated with bone that usually consists of granulation tissue, purulent exudates, and islands of non-vital bone (sequestra). |
22
|
Acute pulpitis
|
An inflammation of the pulp
caused by injury to the pulp, usually from dental caries or trauma. The thermal change (hot or cold) initiates the pain that is relived on removal of the noxious stimuli. It is usually either reversible or irreversible. |
23
|
Addison´s disease
|
A rare
hormonal disorder that occurs when the adrenal glands do not produce enough of the hormone cortisol and less commonly aldosterone. |
24
|
Adenoid squamous cell carcinoma
|
A rare low grade
histopathological variant of oral squamous cell carcinoma or in sun-exposed skin of the face and lower lip. The malignant cells are arranged in a gland like pattern. |
25
|
Adenoma
|
In Clinical
terms refers to a glandular malignancy either benign or malignant. |
26
|
Adenomatoid odontogenic tumor
|
An odontogenic tumor arising
from epithelium and ectomesenchyme, well-circumscribed lesion that usually occurs around the crowns of unerupted anterior teeth of young patients and consists of epithelium in swirls and ductal patterns interspersed with spherical enamel like calcifications. |
27
|
Adenosquamous carcinoma
|
A rare,
aggressive squamous cell carcinoma of the oral mucosa consisting of a mixture of malignant squamous and glandular cells. |
28
|
Adult monostotic fibrous dysplasia
|
A rare form of fibrous dysplasia
occurring spontaneously in adulthood involving a single bone. |
29
|
Adventious dentin
|
The
pathologically formed secondary dentin as a result of abnormal irritation. |
30
|
Aerodontolgia
|
A condition similar to
pulpitis experienced in deep fillings in high altitudes is referred as aerodontalgia. |
31
|
Agenesis
|
Complete
absence of an organ and its associated structures. |
32
|
Agranulocytosis
|
A marked decrease in the
number of granulocytes (circulating or immature), particularly neutrophils. |
33
|
Allergen
|
A substance
capable of inducing hypersensitivity or an allergic reaction. |
34
|
Allergy
|
A hypersensitive state
acquired through exposure to a particular allergen. Re-exposure to the same allergen elicits an exaggerated reaction. |
35
|
Alveolar cyst of new born
|
They are
small, superficial keratin filled cyst found in the alveolar mucosa of infants that arise from the remnants of the dental lamina. |
36
|
Alveolar osteitis
|
The destruction of initial
clot usually after a traumatic extraction prevents the normal healing process causing the clinical condition of alveolar ostetits. Also known as dry socket. |
37
|
Amalgam tattoo
|
Oral soft
tissue discolorations due to amalgam; most common exogenous pigmentation of the oral cavity. |
38
|
Ameloblastic carcinoma
|
An aggressive neoplasm of the
jaws in which the epithelial cells exhibit histologic features of common ameloblastoma and malignancy. |
39
|
Ameloblastic fibroma
|
An
odontogenic tumor arising from epithelium and ectomesenchyme, that is well circumscribed often located over unerupted molars in young patients; the connective tissue recapitulate primitive ectomesenchyme often found during various stages of odontogenesis. |
40
|
Ameloblastic fibro-odontoma
|
An odontogenic tumor arising
from epithelium and ectomesenchyme, that has general features of ameloblastic fibroma but contains enamel and dentin. Alternatively it is an expansile odontogenic tumor in young patients that contains the soft tissue components of ameloblastic fibroma and the hard tissue components of complex odontoma. |
41
|
Ameloblastic odontoma or odontoameloblastoma
|
A rare
odontogenic tumor that contains an ameloblastomatous component together with odontoma-like elements. |
42
|
Ameloblastoma
|
A unicentric neoplasm of
odontogenic epithelium that is clinically benign, anatomically persistent, locally invasive and that has a wide spectrum of histologic patterns. |
43
|
Amelogenesis
|
The process
of formation of the enamel portion of the tooth. |
44
|
Amelogenesis imperfecta
|
A spectrum of hereditary
defects in the formation of ameloblasts and the mineralization of enamel matrix that results in teeth with multiple generalized abnormalities affecting the enamel layer only. |
45
|
Amino acid
|
An organic
compound containing the amino group NH2. Amino acids are the main component of proteins. |
46
|
Amyloidosis
|
Represents a heterogeneous
group of conditions characterized by the deposition of an extra cellular proteincious material called amyloid. |
47
|
Anachoretic pulpitis
|
Refers to the
inflammation of pulp caused by agents reaching pulp through circulation. |
48
|
Anaphylaxis
|
A type of hypersensitivity or
allergic reaction in which the exaggerated immunologic reaction results from the release of vasoactive substances such as histamine. The reaction occurs on re-exposure to a foreign protein or other substance after sensitization. |
49
|
Anaplasia
|
Lack of
differentiation of cells |
50
|
Anaplastic
|
Refers to an adult cell that
has changed irreversibly toward more primitive cell types and is often malignant. |
51
|
Anemia
|
A
quantitative and or qualitative reduction of hemoglobin in blood. (Or) Reduction to less than normal of the number of red blood cells or quantity of hemoglobin or to the volume of packed red blood cells in the blood. (Or) Reduction in oxygen carrying capacity of blood. |
52
|
Anesthesia dolorosa
|
An uncommon side-effect of
surgical treatment of trigeminal neuralgia resulting in a combination of anesthesia and spontaneous pain of the facial skin. |
53
|
Aneurysmal bone cyst
|
An uncommon
lesion (Pseudocyst) located primarily in the posterior mandible and maxilla with clinical features similar to central giant cell lesion often containing many large blood-filled spaces separated by connective tissue septa containing giant cell tissue and lined by epithelium. |
54
|
Angiolipoma
|
A benign tumor that consists of
an admixture of mature fat and numerous small blood vessels. |
55
|
Angioma
|
A benign
tumor made up of blood or lymph vessels. |
56
|
Angiomatosis
|
The process of subcutaneous
vascular proliferation is referred to as angiomatosis. |
57
|
Angioneurotic odema
|
A diffuse
edematous swelling of subcutaneous or submucosal soft tissues and is related to changes in vascular permeability due to mast cell granulation or C1 esterase deficiency. |
58
|
Angiosarcoma
|
Malignant, rare, rapidly
growing lesion of endothelial cells that is more common in young patients and has a poor prognosis. |
59
|
Angular chelitis
|
It is an
infectious diseases occurring along the corners of mouth caused by Candida, staphylococci or streptococci or a mixed infection. The lesion ulcerates and readily bleeds. |
60
|
Anitschkow cell
|
The cytologic smear of a
recurrent apthous ulcer show a characteristic change in nucleus of epithelium with elongated nuclei containing a linear bar of chromatin. Such a cell is termed as Anitschkow cell. |
61
|
Ankyloglssia
|
A
developmental anomaly of tongue characterized by an abnormal extensive adhesion of the tongue to the floor of the mouth or the lingual aspect of the anterior portion of the mandible caused by a short lingual frenum. |
62
|
Ankylosed teeth
|
Teeth that are fused to the
alveolar bone by means of cementum; a condition especially common with retained deciduous teeth. |
63
|
Anodontia
|
Congenital
condition in which all the teeth fail to develop. |
64
|
Anomaly
|
Any deviation from normal. May
involve in composition, number, size, shape or structure. |
65
|
Antibody
|
A protein
produced in the body in response to stimulation by an antigen. Antibodies react specifically to antigens in an attempt to neutralize these foreign substances. |
66
|
Antigen
|
A substance, usually a
protein, which is recognized as foreign by the body’s immune system and stimulates formation of a specific antibody to the antigen. |
67
|
Antoni A tissue
|
In
neurilemoma, some of the neural tissue is regularly arranged in streaming fascicles of Schwann cells which often are palisaded and regularly arranged, refered as Antoni A tissue. |
68
|
Antoni B tissue
|
In neurilemoma, a part of the
neural tissue is irregularly arranged in streaming fascicles of Schwann cells which often are less organized and less cellular refered as Antoni B tissue. |
69
|
Apert’s syndrome or Acrocephalosyndactyly
|
A rare
craniosynostosis syndrome with characteristic features including acrobrachycephaly, Kleeblattschadel (clove leaf) deformity and syndactyly of second, third and fourth digits of limbs observed. |
70
|
Apical peridontal cyst
|
An odontogenic cyst of
inflammatory origin that is preceded by dental caries and a chronic periapical granuloma and stimulation of rests of Malassez present in the periodontal membrane. |
71
|
Aplasia
|
Absence of an
organ owing to lack of division of cells resulting in absence in that particular cells. Or Absence of an organ or a part of an organ due to failure of development of the embryonic tissue of origin or a defect in synchronous growth or a signaling molecule. |
72
|
Aplastic anemia
|
A rare type of life threatening
hematological disorder characterized by failure of the hematopoeitic precursor cells to produce all blood cells, caused usually by the exposure to certain drugs, virus and carcinogens. |
73
|
Apthous ulcer
|
A recurrent
ulcer of uncertain etiology. The chief etiological agents suggested include viruses, stresses and allergy. Includes a solitary large major variant and a multiple small minor variant. |
74
|
Arrested caries
|
A dental caries that has
become static and does not show any tendency for further progression. |
75
|
Asteroid bodies
|
The
granulomatous inflammation of sarcoidosis contains laminated stellate inclusions called as asteroid bodies. |
76
|
Asymptomatic
|
A lack of symptoms or
complaints by the patient. |
77
|
Atrophic
|
A normally
developed tissue that has decreased in size as compared to its normal size. |
78
|
Atrophy
|
Shrinkage in size of cell due
to loss of cell substance. |
79
|
Attrition
|
A regressive
alteration of tooth structure usually involving hard tissue of the permanent dentition leading to loss of tooth structure due to mechanical action of mastication. Is a physiological process when involving aged individuals and pathological in young patients. |
80
|
Atypical
|
Irregular, not conformable to
the type. |
81
|
Auspitz sign
|
A Clinical
sign in psoriasis wherein when the dry scales are removed forcefully reveals a one or more tiny bleeding spots. |
82
|
Autoantibody
|
An antibody that reacts
against an antigenic constituent of the person’s own tissues. |
83
|
Autoimmune disease
|
A disease or
a lesion characterized by tissue injury caused by a humoral or cell-mediated immune response against constituents of the body’s own tissues. |
84
|
Autoimmunity
|
Immune-mediated destruction of
the body’s own cells and tissues; immunity against self. |
85
|
Autoinoculation
|
To inoculate
with a pathogen such as a virus from one’s own body. |
86
|
Autosomes
|
The non-sex chromosomes those
are identical for men and women. |
87
|
B lymphocyte
|
A lymphocyte
-B cell (B for Bursa of fabricus in birds), that forms in bone marrow and matures without passing through the thymus. It matures into plasma cells that produce antibodies or Immunoglobulins. |
88
|
Baby bottle syndrome
|
See Rampant caries
|
89
|
Bacillary angiomatosis
|
Is a
multifocal subcutaneous vascular proliferation associated with cat scratch disease and often observed in patients with long standing HIV infection. They respond to erythromycin. |
90
|
Ballooning degeneration
|
The virus (Simplex virus)
infected cell exhibit acantholysis, nuclear clearing and enlargement and is called as the ballooning degeneration. |
91
|
Basal cell carcinoma
|
A common,
locally invasive, slow spreading, non metastasizing primary epithelial malignancy of the basal layer of skin and its appendages composed of medullary pattens of basaloid cells. |
92
|
Basaloid squamous cell carcinoma
|
Rare, aggressive form of
poorly differentiated oral squamous cell carcinoma consisting of medullary patterns of cells with central areas of necrosis and resembles to basal cell carcinoma of skin. |
93
|
Bell’s palsy
|
Is an acute,
often unilateral paralysis of the facial musculature with no proven cause. |
94
|
Benign
|
Not malignant; favorable for
recovery. |
95
|
Benign fibro-osseous lesions
|
A
heterotrophic collection of non-neoplastic intraosseous lesions that replaces normal bone and consists of a cellular fibrous connective tissue within which nonfunctional osseous structures form. |
96
|
Benign fibrous histiocytoma
|
A diverse group of benign
neoplasm that exhibit both fibroblast and histiocytes and characterized by a storiform pattern with the spindle shaped fibroblast with vesicular nuclei predominating. |
97
|
Benign lymphoepithelial cyst
|
A
lymphoepithelial cyst commonly located intraorally on the posterior lateral tongue and the anterior floor of the mouth inside the lymphoid tissue and is usually submucosal in its position. |
98
|
Benign migratory glossitis
|
A developmental anomaly of
tongue characterized by multiple sensitive irregularly shaped erythematous patches on the tongue with arcuate white rims that enlarge and change shape daily. |
99
|
Bifid condyle
|
Is a rare
developmental anomaly of head & neck region characterized by a double headed mandibular condyle. Fractures of condyle during growth may lead to bifid condyle. |
100
|
Bifid uvula
|
Is the most minimal
manifestation of cleft palate and is limited to soft tissue structure of the uvula. |
101
|
Biopsy
|
Excision of a
living tissue for the purpose of examination by a pathologist. |
102
|
Black hairy tongue
|
Is a developmental defect of
tongue, characterized by marked accumulation of keratin on the filliform papillae of the dorsal aspect and associated with other conditions. |
103
|
Blanching
|
To take the
color out of / Make white. |
104
|
Bleopharochalasis
|
Refers to the recurring edema
of the upper eyelids leading to sagging of the lid at the outer canthus of the eye. It is a major component of the Ascher’s syndrome. |
105
|
Blue nevus
|
A benign
pigmented epithelial pathology that presents as a dark blue dome-shaped papule or as a flat macule on the skin or mucosa. Made up of nevus cell and appears blue due to tyndallization effect. |
106
|
Bohn’s nodules
|
An uncommon superficial raised
nodule scattered over the hard palate often near the border with the soft palate in infants that resolve without treatment; derived from rests of the dental lamina and consisting of keratin-producing epithelial lining. |
107
|
Bony
|
Composed of
or containing bone. |
108
|
Botryoid odontogenic cyst
|
A slow-growing, non-expansile
developmental odontogenic cyst derived from rests of the dental lamina resembling a bunch of grapes. The cyst contains an embryonic lining of 1 to 3 cuboidal cells and distinctive focal thickenings (plaques). |
109
|
Branchial cleft cyst
|
An unusually
large lymphoepithelial cyst located on the lateral aspect of the neck. |
110
|
Brodie´s abscess
|
A chronic abscess walled off
in a sclerotic bone. |
111
|
Bruxism
|
A
parafunctional masticatory habit related to stress or a sleep disorder, characterized by grinding one’s teeth. May lead to attrition. |
112
|
Buccal bifurcation cyst
|
A cyst of uncertain origin
found primarily on the distal or facial aspect of a vital mandibular third molar, consisting of intensely inflamed connective tissue and an epithelial lining. |
113
|
Bulimia
|
A
psychiatric compulsive eating disorder characterized by episodic eating of large volumes of food, followed by purging behavior such as self-induced vomiting. This may cause erosion of the lingual aspect of mandibular anterior teeth. |
114
|
Bull’s eye lesion
|
Skin or mucous membrane
lesions which are concentric rings resembling a circle within a circle; with a slightly depressed, dusky purple center, an elevated, surrounding macular erythema pale middle zone, and an erythematous border; usually associated with herpes simplex or erythema multiforme or drug eruption or mycoplasma infection. |
115
|
Bulla (bullous/ bullae)
|
A
circumscribed elevated blister like lesion that is more than 5 mm in diameter, usually contains serous fluid. |
116
|
Cabots rings
|
A red blood cell abnormal
feature observed in peripheral smear of pernicious anemia. |
117
|
Café au lait spots
|
Hyperpigmented lesions that may vary in
color from light brown to dark brown. The borders may be smooth or irregular. Often found with fibrous dysplasia, neurofibromatosis and certain endocrine abnormalities. |
118
|
Calcifying epithelial odontogenic tumor
|
An odontogenic tumor arising
from epithelium which is locally aggressive consisting of strands and medullary patterns of squamous and clear cells that are often accompanied by spherical calcifications (“Lisegang” ring) and amyloid-staining hyaline deposits. Also known as “Pindborg tumor” |
119
|
Calcifying odontogenic cyst
|
A rare,
well-circumscribed, solid or cystic lesion derived from odontogenic epithelium that superficially resembles follicular ameloblastoma but contains “ghost cells” and spherical calcifications. |
120
|
Cancrum oris
|
Is rapidly progressive
opportunistic infections of the normal oral flora during immunocompromised state and often begins as ANUG. |
121
|
Candidiasis
|
Encompasses a
group of mucosal and cutaneous conditions with a common etiologic agent from the Candida genus of fungi; the most common oral mycotic infection. |
122
|
Canker sores
|
Also known as apthous
stomatitits. It is a most common oral pathological ulceration attributed to many reasons. May present as a major, minor and recurrent forms. |
123
|
Cannon’s disease
|
See white
spongy nevus |
124
|
Capedont teeth
|
Is a term given to teeth
affected with dentinogenesis imperfecta. |
125
|
Capsule
|
Compressed
fibrous connective tissue around a benign tumor or a cyst separating it from surrounding tissues. |
126
|
Carcinogen
|
A cancer causing agent.
|
127
|
Carcinogenesis
|
The train of
biological events that underlies development of neoplasia. |
128
|
Carcinoma
|
A malignant growth made up of
epithelial cells that are capable of infiltration and metastasis. |
129
|
Carcinoma in situ
|
The most
severe stage of epithelial dysplasia, involving the entire thickness of the epithelium, with the epithelial basement membrane remaining intact. |
130
|
Caries, dental
|
The microbial disease of teeth
involving progressive demineralization of inorganic parts of tooth and followed by dissolution of organic material and modified by the saliva and dietary factors. |
131
|
Carotid artery syndrome
|
Is an
abnormal developmental defect caused by the elongation of styloid process and or mineralization of stylohyoid ligament that leads to facial pain, dysphagia and transient syncope. Also known as Eagle’s syndrome. |
132
|
Carotid body tumor
|
Are the tumors that arise from
the carotid body (chemoreceptors responsible for detecting changes in blood pH/ oxygen tension, at the bifurcation of carotids). |
133
|
Carpet tack lesions
|
In discoid
lupus erythematosus, when the cutaneous scales are forcefully removed numerous extensions that had dipped in to the enlarged pilosebaceous canals. Such a lesion is described as carpet tack lesion. |
134
|
Carrier
|
In genetics, a heterozygous
individual who is clinically normal but who can transmit a recessive trait or characteristic; also, a person who is homozygous for an autosomal dominant condition with low penetrance. |
135
|
Cell-mediated immunity
|
Immunity in
which the predominant role is played by T lymphocytes. |
136
|
Cellulitis
|
A painful swelling of the soft
tissue of the mouth and face resulting from a diffuse spreading of purulent exudate along the fascial planes that separate the muscle bundles. |
137
|
Cementifying fibroma
|
Also known as
ossifying fibroma, cemento –ossifying fibroma. It is a well demarcated, osteogenic neoplasm that is composed of fibrous tissue that contain variable amount of calcified structure- bone and cementum in varying proportion. |
138
|
Cementoblastoma
|
A benign, well-circumscribed
neoplasm of cementum-like tissue growing in continuity with the apical cemental layer of a tooth (often molar or premolar) that produce expansion of cortical plates and pain. |
139
|
Cementoma, Familial gigantiform
|
Is a synonym
used for florid type of cemento-osseous dysplasia that occurs in a familial pattern as an autosomal inherited condition. |
140
|
Cemento-osseous dysplasia
|
Are a group of common
fibro-osseous lesions in the jaw that have pathologic features similar to fibrous dysplasia. |
141
|
Cemento-osseous dysplasia, florid
|
A variant of
cemento-osseous dysplasia that is found in the adult females and commonly in the afroamericans. |
142
|
Cemento-osseous dysplasia, Focal
|
A variant of cemento-osseous
dysplasia that is found in the mandibular posterior region, usually in the middle aged females and with no racial predilection. |
143
|
Cemento-osseous dysplasia, periapical
|
A variant of
cemento-osseous dysplasia that is found in the mandibular anterior periapical region, usually in the middle aged females and commonly in the afroamericans. |
144
|
Cemento-ossifying fibroma
|
A well-demarcated,
encapsulated, expansile lesion of the jaws composed of cellular fibrous tissue containing spherical calcifications and irregular, randomly oriented bony structures and may be central or peripheral in location. |
145
|
Central
|
In Oral
Pathology, a lesion occurring within Jaws. |
146
|
Central giant cell lesion
|
An intraosseous destructive
lesion of the jaws in which lesions tends to expand the cortical plates, cause movement of teeth, and produce root resorption; composed of multinucleated giant cells in a background of mononuclear fibro-histiocytic cells and red blood cells. The cause may involve an abnormal calcium metabolism including renal and parathyroid gland pathology. |
147
|
Central odontogenic fibroma
|
An
intraosseous benign neoplasm tissue of odontogenic origin (ectomesenchyme with or without epithelium) containing widely scattered islands and strands of embryonic odontogenic epithelium and calcifications. |
148
|
Central papillary atrophy of tongue
|
A form of erythematous
candidal infection in the central part of the dorsum of tongue. Presents as a well demarcated erythematous zone that is often asymptomatic. It was previously thought to be a developmental anomaly of tongue. |
149
|
Centromere
|
The
constricted portion of the chromosome that divides both the arms. |
150
|
Cervical enamel projection
|
Focal apical extensions of the
enamel beyond the normally smooth cervical margin and on to the root of the tooth. |
151
|
Chanchre
|
Refers to
the lesion of primary syphilis. Develops at the site of inoculation as a papular lesion with a central ulceration. |
152
|
Cheesy
|
Lesion’s texture is similar to
curds of cheese. |
153
|
Chemotaxis
|
Taxis or
movement in response to chemical stimulation. Often exhibited by the phagocytes. |
154
|
Cherubism
|
An autosomal dominant rare
developmental fibro-osseous type of lesion of the jaws in children involving more than one quadrant and stabilizes after the growth period, usually leaving some facial deformity and malocclusion. |
155
|
Chlorodontia
|
A type of intrinsic
greenish discoloration of teeth caused by accumulation of bilirubin that breaks in to biliverdin. This is formed during conditions hyperbilirubinemia. |
156
|
Chondrosarcoma
|
An uncommon malignant bone
neoplasm in the jaws, usually of the anterior maxilla, consisting of a proliferation of chondroblasts or spindle-shaped mesenchymal cells and abnormal cartilage but no osteoid or bone. |
157
|
Choriostomas
|
Ectopic rests
of non transformed tissues, not indigenous to that particular site. Or Is a tumor like growth of microscopically normal tissue in an abnormal location. |
158
|
Chromatid
|
Either of the two vertical
halves of a chromosome that are joined at the centromere. |
159
|
Chromatin
|
A general
term used to refer to the material (DNA) that forms the chromosomes. |
160
|
Chronic
|
Persisting over a longer
duration; generally implies that there has been little change or extremely slow progression over a long period. |
161
|
Chronic apical pulpitis
|
An
irreversible lesion located at the root apex showing the extension of the inflammatory process from the pulpal chamber. (Clinical; Radiological) |
162
|
Chronic hyperplastic pulpitis (pulp polyp)
|
An uncommon and specific type
of inflammatory hyperplasia reaction of pulp to deep caries in a young person in which an inflamed hyperplastic pulp extends through a large carious lesion of a non-vital tooth. |
163
|
Chronic osteomyelitis
|
Prolonged
inflammation of bone and soft tissues of bone including marrow, almost invariably due to infection. |
164
|
Chronic pulpitis
|
An inflammation of the pulp
caused by injury to the pulp, usually from dental caries or trauma. The thermal change (hot) initiates the pain that is not relived on removing the noxious stimuli. It is usually irreversible and with a dull pain. |
165
|
Chrysiasis
|
Is a common
complication of gold therapy that is manifested as a slate blue discoloration of sun exposed skin. |
166
|
Chvosteks’s sign
|
Is an oral finding observed in
hypoparathyroidism. It is characterized by a twitching of upper lip when the facial nerve is tapped just below zygomatic process. It suggests a latent degree of tetany. |
167
|
Clear cell
|
A cell often
associated with pathological lesions in hematoxycillin and eosin stain and which has a clear cytoplasm with a small peripherally located nucleus often due to accumulation of water, carbohydrate or proteins that do not take the stain. |
168
|
Cleft lip
|
A developmental defect of
middle face characterized by the failure of fusion of median nasal process and maxillary process resulting in soft tissue abnormality. |
169
|
Cleft palate
|
A
multifactorial developmental defect of the palate characterized by a lack of complete fusion of the two lateral portions of the palate, resulting in a communication with the nasal cavity. |
170
|
Cleidocranial dysplasia
|
A rare condition inherited as
an autosomal dominant and characterized by partial or complete absence of the clavicles, defective ossification of the skull, and faulty occlusion due to missing, misplaced, or supernumerary teeth along with high arched palate. |
171
|
Coagulation
|
Refers to
the process of clotting. |
172
|
Codon
|
The vertical sequence of three
bases in DNA that codes for an amino acid. (Genetic) |
173
|
Colley’s anemia
|
Is also known
as thalassemia major. It has a defective hemoglobin synthesis inherited through 2 defective genes for beta globin molecule causing microcytic, hypochromic anemia. |
174
|
Commissure or the angle of mouth
|
The junction of the upper and
lower lips at the corner of the mouth. |
175
|
Compound nevus
|
The nevus
characterized by a proliferation of nevus cells microscopically within the basal cell layer of the surface epithelium and involving the underlying connective tissue. |
176
|
Concrescence
|
A developmental anomaly or
post inflammatory defect involving shape of teeth in which there is union of two adjacent teeth by cementum alone without the confluence of dentin. |
177
|
Condyloma acuminatum
|
Is a virus
induced (HPV 6, 11, 16, 18) proliferation of the stratified squamous epithelium of the genetilia. |
178
|
Condyloma lata
|
Is a benign viral induced
(HPV-2, 4, 40) hyperplasia of stratified squamous epithelium that appears as a painless papule or a nodule with a papillary projections. |
179
|
Congenital
|
Present at,
or existing from the time of birth. |
180
|
Congenital lip pits
|
Autosomal dominant trait
resulting in developmental defects involving the vermilion border of the lower and upper lip either at the central or the commissural area. |
181
|
Consanguinity
|
Blood
relationship. In genetics, the term is generally used to describe marriages among close relatives. |
182
|
Corps rands
|
Refers to the peculiar round
shaped dyskeratotic cells observed in Darrier’s disease. |
183
|
Corrugated
|
Descriptive
term for a surface that appears wrinkled. |
184
|
Cotton roll burn
|
An iatrogenic injury caused by
the oral mucosa become adherent to the dry cotton roll and their rapid removal from the mouth lead to stripping of the epithelium in the area. |
185
|
Crouzon syndrome or Craniofacial dysostosis
|
An uncommon,
autosomal dominant craniofacial disorder characterized by craniosynostosis and dysmorphic facial features. The characteristic features include acrobrachycephaly, Kleeblattschadel (clove leaf) deformity and syndactyly of second, third and fourth digits of limbs observed. |
186
|
Crowe’s sign
|
Axillary freckling is known as
crowe’s sign and observed in neurofibromatosis. |
187
|
Cyst
|
Is a
pathologic epithelium-lined cavity, usually containing fluid or semisolid or gas. (Kramer) |
188
|
Cystic hygroma
|
Anomaly of the lymphatic
system characterized by single or multiple cysts within the soft tissues, usually involving the head and neck. |
189
|
Cytologic
|
Pertaining to
the scientific study of cells. |
190
|
Cytology
|
The scientific study of
structures within the cell. |
191
|
Cytopathologic
|
Pertaining to
or characterized by pathologic changes in cells. |
192
|
Darrier’s disease
|
An uncommon genodermatoses
inherited as an autosomal dominant trait with defect in the adherence mechanism between surface squamous epithelial cell leading to acantholysis and characterized histopathologically by test-tube reteridges, corpsrands and grains. |
193
|
Dead tracts
|
Is a age
related change in dentin, where in due to a trauma the odontoblastic process die and dentinal tubules are filled with air in section that appear as dark in transmitted light. |
194
|
Degeneration
|
Refers to the pathologic
changes with cells which may to a certain extent reversible. |
195
|
Delayed eruption
|
The process
of eruption of deciduous or permanent teeth very lately in relative to the normal age range. |
196
|
Dens evaginatus
|
A developmental anomaly in the
shape of teeth in which a focal area of the crown projects outward and produces what appears as an extra cusp or an abnormal shape to existing cuspal arrangements. Often caused by an evagination of the crown during developmental stage. |
197
|
Dens in dente
|
“A tooth
within a tooth”- A developmental anomaly in the shape of a malformed tooth caused by an invagination of the crown before it is calcified. (Or) An enamel-lined “pouch” extending apically from the lingual surface. It commonly affects maxillary lateral incisor teeth and manifests as an invagination on the lingual surface that may reach the pulp. Also known as Dens invaginatus. |
198
|
Dental fluorosis
|
A condition of enamel
hypoplasia characterized by white chalky spots or brown staining and pitting of teeth due to an increased level of fluoride in affecting enamel matrix formation and calcification by the reaction of fluoride on the process of calcification. |
199
|
Dental transposition
|
A
developmental anomaly characterized by a normal teeth erupting in to an inappropriate position. |
200
|
Denticle
|
A regressive alteration of
teeth characterized by spherical calcification within the dental pulp lying free or attached to the pulpal surface of the tooth |
201
|
Dentigerous cyst
|
A common
developmental type of odontogenic cyst associated with unerupted teeth and is caused by fluid accumulation between the reduced enamel epithelium and the enamel surface, resulting in a cyst in which the crown is located within the lumen and root(s) outside. |
202
|
Dentin dysplasia
|
A hereditary developmental
defect in dentin formation in which the coronal dentin and tooth color is normal; the root dentin is abnormal with a gnarled pattern and associated shortened and tapered roots. |
203
|
Dentinogenesis
|
The formation
of dentin. |
204
|
Dentinogenesis imperfecta
|
A hereditary defect consisting
of opalescent teeth composed of irregularly formed and under mineralized dentin that obliterates the coronal and root pulpal chambers. |
205
|
Denture epulis
|
Is a tumor
like hyperplasia of fibrous connective tissue that develops in association with the flange of an ill fitting denture. |
206
|
Denture sore mouth
|
Or Denture stomatitis. It is
an erythematous or better a chronic atrophic candidiasis localized to denture bearing areas of maxillary denture. |
207
|
Dermatofibroma
|
Or fibrous
histiocytoma. They are a diverse group of soft tissue benign tumors that exhibit both fibroblastic and histiocytic differentiation. |
208
|
Dermoid cyst
|
Is an uncommon developmental cystic
malformation of the midline of the upper neck or the anterior floor of the mouth of young patients, derived from remnants of embryonic skin, consisting of a lumen lined by a keratinizing stratified squamous epithelium and containing one or more skin appendages such as hair, sweat, or sebaceous glands. |
209
|
Desmoplastic fibroma
|
A Benign
diffuse infiltrative proliferation of fibroblasts leading to mature collagen deposition, occurring primarily within the mandible in young patients. A histopathological variant of fibroma. |
210
|
Differential diagnosis
|
A list of possible conditions
that fit the information (history, signs, symptoms, radiological, laboratory and histopathological) derived from the patient |
211
|
Differentiation
|
The
distinguishing of one thing from another. Or It is the extent to which neoplastic cells resemble their cell of origin. |
212
|
Diffuse
|
A term used to describe a
lesion whose borders are not well defined or demarcated and is not possible to detect the exact parameters of the lesion. |
213
|
Dilacerations
|
A
developmental anomaly manifested as an abnormal bend or curve. More commonly occurring in the root of a permanent tooth. |
214
|
Diploid
|
Having two sets of
chromosomes; the normal constitution of somatic cells. |
215
|
Distodens
|
An accessory
molar situated distally is called as distodens or distomolars. |
216
|
Dominant
|
A term often used in genetics.
It means a trait or characteristic that is manifested when it is carried by only one of a pair of homologous chromosomes. |
217
|
Donovan bodies
|
Are the
inclusion bodies in the cytoplasm of large mononuclear phagocyte in case of infection with Granuloma Inguinale, a chronic granulomatous infection. These bodies are tiny, elongated basophilic and arygrophilic rods and present in large numbers. |
218
|
Donovan bodies
|
Are tiny elongated basophilic
and argyrophilic rods in the large mononuclear phagocytes in the intracytoplamc cysts in Granuloma inguinale. |
219
|
Doorthy Reed cell
|
Are the
characteristic typically binucleated (owl eye nuclei) or multinucletated (pennies on plate) with prominent nucleoli in Hodgkins lymphoma. |
220
|
Dorsal
|
Directed toward / situated on
the back surface (opposite of ventral). |
221
|
Double lip
|
A rare
developmental anomaly commonly characterized by a horizontal fold of redundant mucosal tissue located on the inner aspect of the upper lip. May be congenital or acquired. |
222
|
Down syndrome
|
A common chromosomal disorder
caused by the presence of an additional third chromosome in chromosome 21 and presents mild to moderate mental retardation and associated medical and dental problems. |
223
|
Drug induced gingival hyperplasia
|
Increased
amount of gingiva. Generalized increase in the fibrous component of the gingiva in patients who have been taking long term doses of phenytoin, cyclosporine and nifedipine. Persistent dental plaque, calculus (tartar) and gingival irritation increase the severity of the hyperplasia. |
224
|
Dry mouth
|
Decreased saliva production.
Also called as xerostomia. |
225
|
Dry socket
|
A clinical
complication of traumatic tooth extraction. It occurs due to disintegration or loss of the blood clot, resulting in a dry appearance of the exposed bone in the socket. |
226
|
Dysplasia
|
An abnormality of development
of any tissue. It is characterized by the loss of normal cellular architecture. In epithelium it is characterized by a disorderly development. Or A non-neoplastic disorderly growth usually in epithelium. |
227
|
Dystrophic calcifications
|
Ectopic
linear calcification within the pulp chamber of a tooth, the etiology of which is unknown. |
228
|
Eagle syndrome
|
Is an abnormal developmental
defect caused by the elongation of styloid process and or mineralization of stylohyoid ligament that leads to facial pain, dysphagia and transient syncope. Also known as carotid artery syndrome. |
229
|
Eburnation of dentin
|
An arrested
caries of occlusal surface which is large and lacks food retention causing the superficially softened and decalcified dentin is burnished till it takes up a hard brown polished surface. |
230
|
Ecchymosis
|
Large reddish-blue areas in
skin or mucous membrane caused by the escape of blood into the tissues, where it clots. It is commonly referred to as a bruise. Ecchymoses do not blanch on diascopy. |
231
|
Ectodermal
|
relates to
the outermost of the three primitive germ layers of an embryo. Ectodermal derived structures include the skin, hair, nails, oral mucous membrane, and the enamel of the teeth. |
232
|
Ectodermal dysplasia
|
Relates to a group of
inherited disorders where the ectodermal derivatives such as skin, sebaceous glands, hair, enamel and nails are malformed. |
233
|
Edema
|
Abnormal
amounts of fluid in the intercellular spaces, resulting in visible swelling. |
234
|
Edentulous
|
The clinical absence of teeth.
|
235
|
Ehler-Danlos syndrome
|
A group of
inherited disorder of connective tissue that result in an abnormal connective tissue fibers especially collagen. |
236
|
Embryonic
|
Pertaining to the earliest
stage of development of an organism. |
237
|
Emigration
|
The passage
or white blood cells through the endothelium and wall of small blood vessels. |
238
|
Enamel hypoplasia
|
A defect in tooth enamel that
results in less quantity of enamel than normal. |
239
|
Enamel pearl
|
Ectopic
nodular deposits of enamel that primarily occur in the bifurcation or trifurcation areas on the roots of molars. |
240
|
Enanthems
|
Eruptions of mucous membrane.
|
241
|
Endodermal
|
Pertaining to
the innermost of the three primitive germ layers of an embryo. Endodermal structures include the epithelium of the pharynx, respiratory tract (except the nose), and the digestive tract. |
242
|
Entropion
|
In chronic inflammatory
conditions of eye such as cicatrical pemphigoid, conjunctival vesicle heals with scarring leading the eye lids to turn inwards. Such a condition is referred as entropion. |
243
|
Eosinophilic granuloma
|
A
pathological condition that has single or multiple bone lesion without visceral involvement, characterized by proliferation of histiocyte like Langerhans cells often affecting children. |
244
|
Epidermoid cyst
|
Is a common cyst of skin with
a lumen lined by keratinizing stratified squamous epithelium, usually filled with keratin and without skin appendages in the capsule wall. |
245
|
Epidermolysis bullosa
|
Refers to a
heterogeneous group of inherited blistering mucocutaneous disorders with a defect in attachment mechanisms of epithelial cells, either to each other or to the connective tissue. |
246
|
Epithelial dysplasia
|
A disorderly state of
epithelium differentiation process characterized by a combination of individual cell and architectural alterations and is an indicator of the potentially malignant state. |
247
|
Epithelium
|
The cellular
makeup of skin and mucous membranes. |
248
|
Epstein’s pearls
|
Uncommon superficial raised
nodules on the midline of the hard palate of infants that resolve without treatment; derived from rests of the dental lamina and consisting of keratin-producing epithelial lining. |
249
|
Epulis fissuratum
|
A reactive
lesion resulting in proliferation of fibrous connective tissue with an associated chronic inflammation in response to chronic injury such as an ill fitting denture. |
250
|
Erosion
|
The pathological wearing away
of hard tissues of teeth through the action of chemical substances. . Also in histopathology refers to discontinuity or denudation of epithelium above the basal cell layer. |