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Autor:
Dipankar De, Man Updesh Singh Sachdeva, Uma Nahar Saikia, Manoj Gopal Madakshira, Anuradha Bishnoi
Publikováno v:
Indian Journal of Dermatopathology and Diagnostic Dermatology, Vol 7, Iss 2, Pp 57-63 (2020)
Background/Objectives: Only anecdotal case reports or small case series have attempted to study the histomorphology patterns of leukemic infiltration. This study explored the possible association of leukemia cutis with, temporal course of disease, su
Publikováno v:
Indian Journal of Dermatopathology and Diagnostic Dermatology, Vol 7, Iss 2, Pp 92-95 (2020)
Tuberous sclerosis complex (TSC) or Bourneville's disease is a genetic multisystem disorder of multisite hamartomas. Majority of TSC cases are sporadic. TSC typically presents in the first decade of life and has a reported incidence of 1:6000–12,00
Publikováno v:
Indian Journal of Dermatopathology and Diagnostic Dermatology, Vol 7, Iss 1, Pp 2-6 (2020)
Background: Vitiligo is the most prevalent pigmentary disorder occurring worldwide. In most cases, the diagnosis is made by clinical examination alone. The disease status (active/stable) needs to be assessed to make appropriate therapeutic decisions.
Publikováno v:
Indian Journal of Dermatopathology and Diagnostic Dermatology, Vol 7, Iss 1, Pp 16-18 (2020)
Angiolymphoid hyperplasia with eosinophilia (ALHE) is a rare vascular tumor which presents as a dermal papule or a nodule over the head-and-neck region. Histopathologically, there is vascular proliferation in the upper dermis and diffuse lymphocytic
Publikováno v:
Indian Journal of Dermatopathology and Diagnostic Dermatology, Vol 7, Iss 2, Pp 78-80 (2020)
Primary cutaneous mucinous carcinoma is a rare slowly growing neoplasm showing predilection for the head and neck, particularly the eyelids. On occasion, it affects other sites including scalp, face, ear, axillae, thorax, abdomen, groin, foot, hand,
Publikováno v:
Indian Journal of Dermatopathology and Diagnostic Dermatology, Vol 7, Iss 1, Pp 46-48 (2020)
Publikováno v:
Indian Journal of Dermatopathology and Diagnostic Dermatology, Vol 6, Iss 2, Pp 100-103 (2019)
Endogenous ochronosis is a manifestation of alkaptonuria, a rare metabolic disease due to homogentisic acid oxidase deficiency. Darkened urine and arthropathy are the other two components that complete the triad of alkaptonuria. Pigmentation of skin,
Publikováno v:
Indian Journal of Dermatopathology and Diagnostic Dermatology, Vol 6, Iss 2, Pp 89-92 (2019)
Papuloerythroderma (PE) is a rare cutaneous condition characterized by intensely pruritic, papular eruptions sparing major skin folds. These lesions later coalesce to form plaques and potentially evolve into erythroderma. The characteristic sparing o
Publikováno v:
Indian Journal of Dermatopathology and Diagnostic Dermatology, Vol 6, Iss 2, Pp 67-74 (2019)
Background: Genital lichen sclerosus (LS) is a chronic, autoimmune, inflammatory dermatosis of genitalia more common in females than males. Diagnosis of early genital LS is difficult clinically; hence, histopathology may help to confirm the diagnosis
Autor:
Sunanda Mahajan, Mithali Jage
Publikováno v:
Indian Journal of Dermatopathology and Diagnostic Dermatology, Vol 5, Iss 1, Pp 42-47 (2018)
Introduction: Periorbital hyperpigmentation (POH) is a routinely encountered condition in dermatology practice. Studying the clinical features and its correlation with dermoscopy will help in better understanding of patterns of periorbital pigmentati