Linear atrophoderma of moulin over face: An exceedingly rare entity
نویسندگان
چکیده
منابع مشابه
Linear atrophoderma of Moulin: an underrecognized entity
Linear atrophoderma of Moulin (LAM) is an acquired skin condition that manifests in early childhood and adolescence. It likely represents a form of cutaneous mosaicism that presents with linear, hyperpigmented and atrophic lesions appearing on the trunk and limbs. Its clinical appearance varies and may closely resemble that of atrophoderma of Pasini and Pierini (APP) and linear scleroderma. LAM...
متن کاملLinear atrophoderma of Moulin
CASE REPORT A 22-year-old Malay woman presented with an 11-year history of asymptomatic, unilateral brown patches affecting the right arm, right side of the trunk, and right leg. There were no prior skin lesions or inflammation. There was no significant medical or family history. Physical examination found linear hyperpigmented atrophic patches on the right arm, right trunk extending down to th...
متن کاملLinear atrophoderma of Moulin located on the face
Linear atrophoderma of Moulin (LAM) is a dermatosis characterized by hyperpigmented and depressed band-like lesions localized along the Blaschko lines. This dermatosis was described for the first time by Moulin et al. in five patients with similar characteristics in 1992 and referred to atrophoderma of Moulin, with referrance to the first publication [1,2]. Major characteristics of LAM are bein...
متن کاملA case of linear atrophoderma of Moulin.
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متن کاملAn unusual manifestation of linear atrophoderma of Moulin.
the pretibial areas. Erythema ab igne. Arch Dermatol 1990; 126: 386 ± 387. 4. Meffert JJ, Davis BM. Furniture-induced erythema ab igne. J Am Acad Dermatol 1996; 34: 516 ± 517. 5. Butler ML. Erythema ab igne, a sign of pancreatic disease. Am J Gastroenterol 1977; 67: 77 ± 79. 6. Ashby M. Erythema ab igne in cancer patients. J R Soc Med 1985; 78: 925 ± 927. 7. Arrington JH 3rd, Lockman DS. Therma...
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ژورنال
عنوان ژورنال: Indian Journal of Dermatology
سال: 2017
ISSN: 0019-5154
DOI: 10.4103/ijd.ijd_469_16