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Lk Asha
3Publications
2H-index
8Citations
Publications 3
Newest
Mp Binitha2
Estimated H-index: 2
,
Daisy Thomas2
Estimated H-index: 2
,
Lk Asha2
Estimated H-index: 2
Tuberous sclerosis is an autosomal dominant disease due to mutations in two genetic loci, characterized by hamartoma formation in the skin, nervous system, heart, kidney, and other organs. Dyschromatosis universalis hereditaria is an autosomal dominant genodermatosis, characterized by small hyperpigmented and hypopigmented macules, uniformly distributed over the entire body. The face is rarely involved, and the palms, soles, and mucous membranes are usually spared. We report a case of tuberous s...
Published on Jan 1, 2006
Mp Binitha2
Estimated H-index: 2
,
Daisy Thomas2
Estimated H-index: 2
,
Lk Asha2
Estimated H-index: 2
Tuberous sclerosis is an autosomal dominant disease due to mutations in two genetic loci, characterized by hamartoma formation in the skin, nervous system, heart, kidney, and other organs. Dyschromatosis universalis hereditaria is an autosomal dominant genodermatosis, characterized by small hyperpigmented and hypopigmented macules, uniformly distributed over the entire body. The face is rarely involved, and the palms, soles, and mucous membranes are usually spared. We report a case of tuberous s...
Lk Asha2
Estimated H-index: 2
,
Daisy Thomas2
Estimated H-index: 2
+ 1 AuthorsG Nandakumar2
Estimated H-index: 2
A 45-year-old male presented with asymptomatic tumors all over the body. The tumors showed no signs of ulceration or regression. There were generalized, nontender, firm to hard enlarged lymph nodes without hepatosplenomegaly. Biopsy and immunophenotyping revealed CD 30+ anaplastic primary cutaneous large cell lymphoma. Primary cutaneous anaplastic large cell lymphoma is characterized by single or grouped reddish-brown tumor nodules, which frequently tend to ulcerate. Secondary involvement of lym...
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