Nonpustular annular psoriasis is a rare form of psoriasis with clinically annular ring-shaped configuration. In contrast to recurrent circinate erythematous psoriasis, which is the mildest form of pustular psoriasis, no evidence of histopathological Kogoi�s spongiform pustule formation is detected. We report a case of 57-year-old Japanese woman with nonpustular annular psoriasis for 4 year.
Localized myxedema may be observed in hypo/hyperthyroidism [1]. However, the affected sites are usually pretibial area and the lesion on the eye lid is rare. We report a case of myxedema on the bilateral upper eyelids, which was a diagnostic clue of hypothyroidism associated with Hashimoto disease. .
Cutaneous angiosarcoma is an uncommon malignant vascular tumor with a highly variable presentation. It most commonly occurs on the head and neck of elderly Caucasian men, while less commonly on the skin of persons with pre-existing conditions or cutaneous lesions.
India alone, contributes about 58.8% and 81.2% of the newly detected cases of leprosy, globally and in the South East Asian region, respectively [1].
Background: Skin tags are small, soft, pedunculated, often pigmented lesions, usually occurring on the eyelids, neck and axillae. There have been a few reports in the literature that the presence of skin tag is associated with different components of the metabolic syndrome.
Objective: To evaluate the relationship between components of metabolic syndrome (atherogenic lipid, glucose level, hypertension, and waist circumference) and other metabolic associations with skin tags.
The Raynaud's phenomenon (RP) is well known as the first sign of systemic scleroderma (SS) and related disorders. Its early diagnosis leads to a better understanding of the disease and favorable prognosis.
Background: Molluscum Contagiosum is a common viral skin infection, caused by poxvirus, commonly affects young children. Although there is no specific treatment for this infection, many therapeutic modalities has been used with different success rates.
Objectives: To evaluate the effectiveness of topical 20% KOH, 20% KOH with pricking and pricking alone as comparative treatments for molluscum contagiosum.
Vitiligo and melasma are acquired pigmentary disorder of the skin and also the leading cause for dermatologist consultation in South Asian countries like Nepal. Vitiligo vulgaris and melasma are common examples for depigmentary and hyperpigmentary conditions respectively. There are multiple proven medical, surgical and combined modalities of managing them but the challenge in our part of the world with majority of Fitzpatrick skin types III-V is; it remains a psychosocial-cosmetic disease.
A 32-year-old man presented with a history of progressive, painful nodular growths with discharge consisting granules over the right thigh, inguinal area and right foot. Histopathological examination of the tissue biopsy was actinomycotic mycetoma. The patient showed improvement with trimethoprim-sulfamethoxazole. The novelty of our case is to use Co-trimoxazole as a first line treatment modality for cases diagnosed or suspected as actinomycetoma.
Schamberg disease, also known as Schamberg purpura or progressive pigmentary purpura, is characterized by orange-brown or reddish-brown macules/patches with overlaying purpuric spots simulating "cayenne pepper". We report a 54-year-old Chinese woman with Schamberg disease presenting with purpuric macules and patches of varying sizes on the ankles, legs, and knees. The lesions were nonblanchable and nonpalpable and asymptomatic.
Up to 90% of patients with psoriasis develop onychodystrophy at some point during their lives. Nail involvement precedes the skin lesions in approximately 4% of patients. We herewith report a case of a 7-year-old boy with psoriatic onychodystrophy at the age of 6 years followed by the appearance of plaque psoriasis 6 months later. The psoriatic onychodystrophy was initially misdiagnosed as onychomycosis by his family physician and was treated as such.
Annular elastolylic giant cell granuloma (AEGCG) is a rare granulomatous skin disease characterized by loss of elastic fibers accompanied with elastophagocytosis by multinucleated giant cells.
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