Nevus of Ota is a rare pigmented disorder affecting the skin along the distribution of trigeminal nerve. Oral involvement of this pigmented lesion is very rare. Classification of Nevus of Ota given by Tanino represents the skin manifestations well but does not include the extra cutaneous manifestations. Hence an addition to this classification is being proposed through this case report which de...

The pigmentation of human gingival tissue is derived from melanin granules, which are synthesized in the melanosomes of melanocytes [1,2]. The nicotine present in tobacco activates melanocytes to promote melanin secretion [3]. Therefore, the melanin pigmentation in gingival tissues has a strong correlation with smoking [4,5]. In 1977, Hedin et al. [5] first reported that smokers showed more pig...

Dyskeratosis congenita is a rare congenital disorder characterized by a triad of reticular pigmentation of the skin, dystrophic nails, and leukoplakia of the mucous membrane. Sometimes it is associated with bone marrow failure, secondary malignancy and interstitial lung disease. Though it is rare, Dyskeratosis congenita is diagnosed relatively easily when clinicians suspect it. It can be diagno...

Hutchinson - Gilford Progeria Syndrome is a rare genetic disorder characterized by premature aging involving the skin, bones, heart, and blood vessels. We report a three-year-old boy with clinical manifestations characteristic of this syndrome. He had a characteristic "plucked-bird" appearance, prominent eyes and scalp veins, senile look, loss of scalp hair, eyebrows, and eyelashes, stunted gro...

Peutz-Jeghers syndrome is an inherited disorder which usually debuts during childhood. It is characterized by mucocutaneous pigmentation and hamartomatous polyps in the gastrointestinal tract. Numerous reports indicate a high incidence of gastrointestinal and extraintestinal cancer in these patients, their appearance at a young age, as well as its association with ovarian and testicular tumors....

Subungual pigmentation can have benign and malignant etiologies. A common and important differential diagnosis is between subungual hematoma and subungual acrolentiginous melanoma. We have introduced Dr. Eckert Haneke's technique and our Hydrogen Peroxide modification for distinguishing these entities clinically. Dr. Haneke's technique uses the hemocult reaction to detect hematoma from the spec...

Dyskeratosis Congenita (DC) is a rare inherited disorder of ectodermal dysplasia. It consists of a classical mucocutaneous triad of abnormal skin pigmentation, nail dystrophy and leukoplakia. Pulmonary disease is seen in 10-15%. It is characterized by Idiopathic Pulmonary Fibrosis (IPF), or Idiopathic Familial Pulmonary Fibrosis (IFPF). Non-specific Interstitial Pneumonia (NSIP) has been report...

Gorlin-Goltz syndrome is a rare autosomal dominant disorder that involves multiple organ systems, including the skin, skeleton and jaws. We report a case of young female with multiple odontogenic keratocysts, high arched palate, euryopia, palmer pits, solitary, pigmented nevus , areas of hyper-pigmentation in the upper eyelid of left eye, dorsal surface of hands, calcified diaphragma sellae, ri...

Dyskeratosis Congenita (DC) is a rare inherited fatal disorder characterized by classic triad of oral leukoplakia, nail dystrophy and abnormal skin pigmentation. Variable somatic abnormalities may be present like pulmonary, neural, immune, oral complications. Bone marrow failure, pulmonary disease and malignancy are the main mortality causes of disorder. Oral and dental manifestations could be ...

OBJECTIVE Passive smoking leads to melanin pigmentation on gingiva. However, documentation of gingival pigmentation and salivary amylase activity in passive smokers relative to the duration of exposure to environmental tobacco smoke (ETS), is incomplete and requires further investigation. Thus, this study aimed to assess effects of ETS exposure on gingival pigmentation in young adults. In addit...