Ecchymosis-like hyperpigmented mycosis fungoides

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Hyperpigmented mycosis fungoides: a rare variant

Mycosis fungoides (MF) is the most common type of cutaneous Tcell lymphoma. The diagnosis of classic MF is based on a combination of clinical presentation, histopathology, immunohistochemistry, and T-cell monoclonality detected by molecular studies. However, the diagnosis can be difficult in some cases. We report a case of hyperpigmented mycosis fungoides. A 60-year-old woman, phototype IV, pre...

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Mycosis fungoides with unusual vitiligo-like presentation.

Mycosis fungoides (MF), the commonest variant of primary cutaneous T cell lymphoma (CTCL), is relatively uncommon among the Asians. Hypopigmented mycosis fungoides is a rare variant usually observed in dark-skinned individuals, especially children. Hypopigmented MF usually responds well to therapy, particularly to PUVA, and has a comparatively benign course. Mycosis fungoides in a 16-year-old b...

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folliculotropic mycosis fungoides with comedonal-like appearances

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[Mycosis fungoides].

History A middle-aged male with a 10-year-history of generalized pruritus involving the whole body was seen in a skin clinic. He denied any significant past medical or drug history. He had no known allergy. Previous skin biopsy performed over the abdomen in February 1999 showed features of lichen planus. He was treated with various topical steroids, emollients and antihistamines but the skin ra...

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Increasing Numbers of Mast Cells in Skin Lesions of Hyperpigmented Mycosis Fungoides with Large-Cell Transformation.

Vol. 28, No. 1, 2016 115 Received October 24, 2014, Revised March 2, 2015, Accepted for publication March 21, 2015 Corresponding author: Ken Igawa, Department of Dermatology, Tokyo Medical and Dental University, Graduate School of Medicine, Yushima 1-5-45, Bunkyo-ku, Tokyo 1138519, Japan. Tel: 81-3-5803-5286, Fax: 81-3-5803-0143, E-mail: [email protected] This is an Open Access article dis...

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ژورنال

عنوان ژورنال: Annals of Saudi Medicine

سال: 2008

ISSN: 0256-4947,0975-4466

DOI: 10.5144/0256-4947.2008.228