Reticulate acropigmentation of Kitamura (RAK) is a rare genetic disorder of cutaneous pigmentation with an autosomal dominant pattern of inheritance and a high penetration rate. The characteristic skin lesions are reticulate, slightly depressed pigmented macules mainly affecting the dorsa of the hands and feet, which first appear before puberty and subsequently expand to the proximal limb and t...

Journal of Cutaneous and Aesthetic Surgery ¦ Volume 10 ¦ Issue 1 ¦ January‐March 2017 60 Subungual SCC is a low‐grade malignant tumour with >150 cases reported in literature. It may arise from nail bed, matrix, groove or nail folds.[2] It usually affects elderly males with thumb being the most common site of involvement.[3] Early clinical manifestations are paronychia, onychomycosis, onycholysi...

Epidermolysis bullosa simplex with mottled pigmentation (EBS-MP) is a rare subtype of EBS. It characterized by non-cicatricial blisters, mainly at the distal extremities, and progressive hyperpigmentation. Its clinical features depend on age diagnosis, variations have been described even within family members. Blisters usually appear birth or in early infancy, tend to decrease age, only occasio...

Vol. 27, No. 2, 2015 235 Received March 13, 2014, Revised May 14, 2014, Accepted for publication June 23, 2014 Corresponding author: Jee-Bum Lee, Department of Dermatology, Chonnam National University Hospital, 42 Jebong-ro, Dong-gu, Gwangju 501-757, Korea. Tel: 82-62-220-6684, Fax: 82-62-222-4058, E-mail: [email protected] This is an Open Access article distributed under the terms of the Creati...

Degos-like lesions (DLL) have been associated with connective tissue diseases. Till date only twelve cases of systemic lupus erythematosus (SLE) DLL published. We describe a rare case SLE leg ulcers and DLL. A 23-year-old male presented malar rash, photosensitivity, ulcers, joint pain, oral altered sensorium dyspnea. Cutaneous examination also revealed atrophic, porcelain-white scars over body ...

Degos' disease, or malignant atrophic papulosis, is a rare and often fatal multisystem vasculopathy of unknown etiology. The cutaneous manifestations comprise erythematous papules, which heal to leave scars with a pathognomonic central porcelain-white atrophic area and a peripheral telangiectatic rim. Involvement of the gastrointestinal tract is observed in 50% of cases, with intestinal perfora...

572 Indian Journal of Dermatology 2016; 61(5) 5. Chen JH, Wang KH, Hu CH, Chiu JS. Atypical angioma serpiginosum. Yonsei Med J 2008;49:509-13. 6. Ohnishi T, Nagayama T, Morita T, Miyazaki T, Okada H, Ohara K, et al. Angioma serpiginosum: A report of 2 cases identified using epiluminescence microscopy. Arch Dermatol 1999;135:1366-8. 7. Ghanadan A, Kamyab-Hesari K, Moslehi H, Abasi A. Dermoscopy ...

Over the last few years, dermoscopy has been shown to be a useful tool in assisting the noninvasive diagnosis of various general dermatological disorders. In this article, we sought to provide an up-to-date practical overview on the use of dermoscopy in general dermatology by analysing the dermoscopic differential diagnosis of relatively common dermatological disorders grouped according to thei...

Malignant atrophic papulosis, commonly known as Degos disease, is a rare vasculopathy encompassing both benign, cutaneous and lethal systemic variants. We report a case of chronic cutaneous lupus erythematosus in a 41-year-old male presenting with prominent Degos-like skin lesions. Multiple atrophic, porcelain-white, scar-like papules and plaques with dusky, erythematous borders, suggestive of ...