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Agminated Nevi of the Foot with Checkerboard and Blaschkoid Distribution.
Dermatol Pract Concept
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Anatomic Pathology Unit, Hospital of Macerata, Macerata, Italy.
sQuiz your knowledge: A case of multiple nevi with unilateral segmental agminated distribution.
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Department of Dermatovenereology, Chengdu Second People's Hospital, Chengdu, Sichuan, China.
Novel three-way complex rearrangement of TRPM1-PUM1-LCK in a case of agminated Spitz nevi arising in a giant congenital hyperpigmented macule.
Pigment Cell Melanoma Res
September 2020
Department of Biopathology, Center Léon Bérard, Lyon, France.
The genetic anomalies associated with the agminated variant of Spitz nevus have so far been limited to HRAS G13R mutations, especially when arising within a nevus spilus. A previous report exposed the case of a man with a giant pigmented macule involving his upper right limb and trunk. Since childhood, Spitz nevi have been periodically arising, within the pigmented area.
View Article and Find Full Text PDFCongenital eccrine angiomatous hamartoma: Expanding the morphologic presentation and a review of the literature.
Pediatr Dermatol
November 2019
Division of Dermatology, Department of Pediatric Dermatology, Phoenix Children's Hospital, Phoenix, Arizona.
Eccrine angiomatous hamartoma (EAH) is a rare benign vascular hamartoma characterized histologically by an increased size and number of mature eccrine glands associated with multiple foci of dilated capillaries in the dermis and subcutis. EAH typically presents in children as discrete, solitary nodules, or plaques most commonly located on the extremities. Some cases of EAH have an agminated distribution involving classic locations, or present as solitary lesions in less common locations such as the face, scalp, or trunk.
View Article and Find Full Text PDFCongenital-type juvenile xanthogranuloma: A case series and literature review.
Pediatr Dermatol
September 2018
Department of Dermatology, University of California, San Francisco, CA, USA.
Background/objectives: Congenital juvenile xanthogranulomas are infrequently described in the medical literature. We report three previously unpublished cases and systematically review the literature to better characterize this variant.
Methods: We surveyed English-language articles indexed in MEDLINE (1951-March 2017) and EMBASE (1974-March 2017) for cases of congenital-onset juvenile xanthogranulomas confirmed on histopathology.
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