Epidermal Nevi and Related Syndromes —Part 2: Nevi Derived from Adnexal Structures

Garcías-Ladaria, J.; Rosón, M. Cuadrado; Pascual-López, M.

doi:10.1016/j.adengl.2018.07.020

Cited by 9 publications

(14 citation statements)

References 99 publications

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“…Linear nevus sebaceous syndrome, also known as Schimmelpenning-Feuerstein-Mims syndrome (SFMS) (OMIM 163200) [4], is a rare, sporadic neurocutaneous syndrome characterized by linear sebaceous nevi that follow the lines of Blaschko, in addition to extracutaneous manifestations including the central nervous system, eyes, skeleton, and other organs [5]. Several gene mutations have been identified in the affected skin including HRAS, NRAS [6], and KRAS genes [7].…”

Section: Pathology and Geneticsmentioning

confidence: 99%

“…His genetic testing for tuberous sclerosis was also negative. Other studies have reported extra-neurological manifestations in organs including the eyes (coloboma, strabismus), bone (cranial abnormalities, bone cysts), hypophosphatemic rickets, heart (coarctation of the aorta), kidneys (horseshoe kidney), and growth asymmetry [5,9].…”

Section: Dysmorphology and Extra-neurological Manifestationsmentioning

confidence: 99%

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Linear Nevus Sebaceous Syndrome in a Child With Infantile Spasms and Focal Cortical Dysplasia

Salman

Fathalla

Akbari

2021

Cureus

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Linear nevus sebaceous syndrome (LNSS) is a rare neurocutaneous syndrome with important neurological involvement including brain malformation, focal seizures, and developmental delay. We discuss a case with a unique presentation with localization-related infantile spasms and review the clinical and radiological features of this case. To our knowledge, there are no previously reported cases of LNSS with infantile spasms and cortical dysplasia. Therefore, the presented case will make an important contribution to the available knowledge.

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Section: Pathology and Geneticsmentioning

confidence: 99%

Section: Dysmorphology and Extra-neurological Manifestationsmentioning

confidence: 99%

Linear Nevus Sebaceous Syndrome in a Child With Infantile Spasms and Focal Cortical Dysplasia

Salman

Fathalla

Akbari

2021

Cureus

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“…Nevus sebaceus lesions appear at birth as waxy, yellow-orange or tan, hairless plaques commonly on the scalp with a localized area of alopecia [3]. However, they may also occur on the forehead, face, or neck [2,7]. Lesions range in size from one to several centimeters.…”

Section: B C a Dermatology Online Journal || Case Reportmentioning

confidence: 99%

Nevus sebaceus with syringocystadenoma papilliferum, prurigo nodularis, apocrine cystadenoma, basaloid follicular proliferation, and sebaceoma: case report and review of nevus sebaceus-associated conditions

Basu

Erickson²,

Calame³

et al. 2020

Dermatology Online Journal

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“…Nevus sebaceus (NS) or organoid nevus, also known as the NS of Jadassohn, was first described by Jadassohn in 1895. 1 , 2 NS presents as well-demarcated hamartomatous lesions consisting of mainly sebaceous glands, epidermis, defective hair follicles, and apocrine glands. 2 , 3 About two-thirds of NS cases are diagnosed at birth, while the rest are usually diagnosed in early childhood.…”

Section: Introductionmentioning

confidence: 99%

“… 1 , 2 NS presents as well-demarcated hamartomatous lesions consisting of mainly sebaceous glands, epidermis, defective hair follicles, and apocrine glands. 2 , 3 About two-thirds of NS cases are diagnosed at birth, while the rest are usually diagnosed in early childhood. 4 This condition is most commonly found on the hairy scalp, face, and neck, but rarely presents on the chest and oral mucosa.…”

Section: Introductionmentioning

confidence: 99%

Atypical Nevus Sebaceus at an Unusual Location Treated with Carbon Dioxide Laser: A Case Report

Sutedja¹,

Mareta²,

Sutedja³

et al. 2022

CCID

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Nevus sebaceus (NS) or organoid nevus is an epidermal nevus comprising predominantly sebaceous glands with a prevalence of approximately 0.3% of the newborns. The initial clinical manifestations of NS are single or less commonly multiple yellowish patches with overlying alopecia, usually confined to the scalp. However, it can also appear on the face, preauricular area, and the neck. During puberty, skin lesions will turn into round or linear verrucous plaques accompanied with an increase in number due to the influence of androgens. As they progress, about 20% of the NS cases might turn into secondary tumors which can be benign or malignant (in 2.5% cases). NS can manifest as atypical lesions and may also arise on areas other than its predilection sites. A case of a lesion presented on an atypical location of an 18-year-old male patient treated with carbon dioxide (CO 2 ) laser was reported. Physical examination revealed skin-colored and blackish-brown papules arranged in groups on the left side of the patient’s chest. Histopathological examination on a sample taken from one of the skin lesions on the chest showed hyperkeratosis, acanthosis, papillomatosis, and sebaceous hyperplasia, confirming the diagnosis of NS. The patient was treated with CO 2 laser, and clinical improvements were observed. Histopathological examination of NS is not routinely performed; however, it should be carried out when the lesion is atypical and presented at an unusual location, or there is a suspicion of malignancy.

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Epidermal Nevi and Related Syndromes —Part 2: Nevi Derived from Adnexal Structures

Cited by 9 publications

References 99 publications

Linear Nevus Sebaceous Syndrome in a Child With Infantile Spasms and Focal Cortical Dysplasia

Linear Nevus Sebaceous Syndrome in a Child With Infantile Spasms and Focal Cortical Dysplasia

Nevus sebaceus with syringocystadenoma papilliferum, prurigo nodularis, apocrine cystadenoma, basaloid follicular proliferation, and sebaceoma: case report and review of nevus sebaceus-associated conditions

Atypical Nevus Sebaceus at an Unusual Location Treated with Carbon Dioxide Laser: A Case Report

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