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Naevus lipomatosus superficialis | DermNet
https://dermnetnz.org/topics/naevus-lipomatosus-superficialis
WEBNaevus lipomatosus superficialis is a developmental malformation (a cutaneous hamartoma or type of birthmark ). Two types are described: the classical type (also called Hoffmann-Zurhelle) and the solitary type. Other names for naevus lipomatosus superficialis are superficial lipomatous naevus and fat naevus.
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Nevus Lipomatosus Superficialis - Dermatology Advisor
https://www.dermatologyadvisor.com/home/decision-support-in-medicine/dermatology/nevus-lipomatosus-superficialis/
WEBMar 13, 2019 · Nevus lipomatosis superficialis is usually asymptomatic but rarely associated with with foul smelling discharge, pain or ulceration. The rate of growth is static to slow. Sites of predilection include the pelvic girdle, lumbar area, buttock, and upper thigh, and rarely the scalp, face, nose, neck, shoulder, thorax, genitalia, abdomen, and soles.
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Nevus Lipomatosus - DoveMed
https://www.dovemed.com/diseases-conditions/nevus-lipomatosus
WEBJun 21, 2022 · Learn in-depth information on Nevus Lipomatosus, its causes, symptoms, diagnosis, complications, treatment, prevention, and prognosis.
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Naevus lipomatosus superficialis pathology | DermNet
https://dermnetnz.org/topics/naevus-lipomatosus-superficialis-pathology
WEBAuthors: Assoc Prof Patrick Emanuel, Dermatopathologist, Auckland, New Zealand, 2013. Naevus lipomatosus superficialis is a rare lesion. It is regarded as a connective tissue naevus by most authorities. It can occur as either a single dermal papule or as a cluster of multiple papules and nodules.
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Pathology Outlines - Nevus lipomatosus superficialis
https://www.pathologyoutlines.com/topic/skintumornonmelanocyticnls.html
WEBAug 1, 2012 · Also called nevus lipomatosus cutaneous superficialis and dermolipoma. Not a WHO diagnosis. First described in 1921 by Hoffman and Zurhelle. Considered to be a developmental anomaly or hamartoma. Epidemiology. Uncommon. At birth or by age 20 years. Clinical features. Buttocks or upper thighs.
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Nevus lipomatosus superficialis - Wikipedia
https://en.wikipedia.org/wiki/Nevus_lipomatosus_superficialis
WEBNevus lipomatosus (cutaneous) superficialis ( NLS or NLCS, also known as "Nevus lipomatosis of Hoffman and Zurhelle" [1]) is characterized by soft, yellowish papules or cerebriform plaques, usually of the buttock or thigh, less often of the ear or scalp, with a wrinkled rather than warty surface.
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Nevus lipomatosus superficialis: A rare cutaneous hamartoma
https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3937478/
WEBNevus lipomatosus superficialis is a rare benign idiopathic skin malformation characterized by the presence of ectopic mature adipose tissue in the dermis. The proportion of the fatty tissue varies greatly from more than 50% to < 10% of the dermis. [ 2]
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Nevus lipomatosus cutaneous superficialis - PMC - National …
https://ncbi.nlm.nih.gov/pmc/articles/PMC5682701/
WEBOct 2, 2015 · Abstract. Nevus lipomatosus cutaneous superficialis is a rare benign hamartomatous skin tumor characterized by dermal deposition of mature adipose tissue. Two clinical forms have been described (classical and solitary types). We describe a case of nevus lipomatosus cutaneous superficialis with a 13-year history of growth in a young …
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Nevus Lipomatosus Cutaneous Superficialis: Clinicopathological …
https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9792013/
WEBAbstract. Nevus lipomatosus cutaneous superficialis (NLCS) is a rare cutaneous hamartomatous lesion, histopathologically characterized by the presence of ectopic dermal adipocytes. Herein, reported is the clinicopathological aspect of six cases of NLCS, consisting of three males and three females, with age at presentation ranging from 18 to …
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Nevus Lipomatosus Cutaneous Superficialis: Clinicopathologic
https://journals.lww.com/ijod/fulltext/2022/67040/nevus_lipomatosus_cutaneous_superficialis_.57.aspx
WEBNevus lipomatosus cutaneous superficialis (NLCS) is a rare benign hamartomatous skin lesion characterized by the presence of ectopic mature adipose tissue in the dermis. It was first reported by Hoffmann and Zurhelle, way back in 1921.[ 2 ]
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