Sebaceous nevus syndrome: Report of two cases

Bonioli, E; Bertolag, Antonella; Stefano, Antonio Di; Bellini, Carlo

doi:10.1016/s0887-8994(97)80672-8

Cited by 16 publications

(12 citation statements)

References 7 publications

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“…23 It is the best known ENS, and some authors still prefer to categorize it as ''the ENS.'' [24][25][26][27][28][29][30] The terminology of this birth defect is rather confusing and includes, in addition to Schimmelpenning syndrome, 5,21,31 many other names, such as Feurstein, FeuersteinFeurstein, Feuerstein Mims syndrome, [32][33][34] Schimmelpenning-Feuerstein-Mims syndrome, 35-37 Solomon syndrome, [38][39][40] ENS, 12,38,[41][42][43][44][45][46] Jadassohn nevus phacomatosis, [47][48][49] Jadassohn-Schimmelpenning-Feuerstein-Mims syndrome, 50 organoid nevus phacomatosis, 35,51 organoid nevus syndrome, 52,53 sebaceous nevus syndrome, [54][55][56][57][58] linear sebaceous nevus syndrome, 50,[59][60][61][62][63][64] and Jadassohn sebaceous nevus syndrome. 65 Consequently, Schimmelpenning syndrome temporarily had three different Online Mendelian Inheritance in Man numbers; these have resently been reduced to two entries (163200 and 601359).…”

Section: Schimmelpenning Syndromementioning

confidence: 99%

The group of epidermal nevus syndromes

Happle

2010

Journal of the American Academy of Dermatology

208

171

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Section: Schimmelpenning Syndromementioning

confidence: 99%

The group of epidermal nevus syndromes

Happle

2010

Journal of the American Academy of Dermatology

208

171

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“…10 Histologically they may be lipomas, fibrolipomas, angiofibromas or hamartomata consisting of fatty and cartilaginous tissue. [12][13][14][15][16][17][18][19] It is worth recalling that many authors regard Haberland syndrome as a localized form of Proteus syndrome, from which the former differs by virtue of the fact that the skin lesions are restricted to the head, are unilateral and do not evolve. [3][4][5][6][7]10 Histological findings include dermal fibrosis with a variable increase in subcutaneous fat.…”

Section: Discussionmentioning

confidence: 99%

Encephalocraniocutaneous lipomatosis (Haberland syndrome) with bilateral cutaneous and visceral involvement

Rubegni¹,

Risulo²,

Sbano³

et al. 2003

Clinical and Experimental Dermatology

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Encephalocraniocutaneous lipomatosis, or Haberland syndrome, is a rare congenital neurocutaneous disease. It is characterized clinically by unilateral lipomatous hamartomata of the scalp, eyelid, and outer globe of the eye, ipsilateral porencephalic cysts with cortical atrophy, cranial asymmetry, marked developmental delay and mental retardation. This syndrome should be distinguished from other mosaic neurocutaneous phenotypes such as as Delleman syndrome, Schimmelpenning syndrome, Goltz syndrome, Goldenhar syndrome and Proteus syndrome. Here we report a case of Haberland syndrome with bilateral involvement which underscores the extreme heterogeneity of clinical presentation of this and related syndromes.

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“…Besides this term, we find in the literature the following synonymic designations: Schimmelpenning syndrome [19, 20, 21, 22]; Feuerstein-Mims syndrome [6, 7, 23]; Schimmelpenning-Feuerstein-Mims syndrome [11, 24, 25]; epidermal nevus syndrome of Solomon [26, 27, 28]; epidermal nevus syndrome of Solomon, Fretzin and Dewald [29]; Solomon syndrome [10]; linear nevus sebaceus syndrome [30, 31, 32, 33, 34]; sebaceous nevus syndrome or nevus sebaceus syndrome [35, 36, 37, 38]; organoid nevus phacomatosis [2, 24, 39]; organoid nevus syndrome [40, 41]; Jadassohn disease [42]; Jadassohn sebaceous nevus syndrome [43], and Jadassohn nevus phacomatosis [44, 45]. As a consequence of this confusing nomenclature, Schimmelpenning syndrome even has two different OMIM entries (no.…”

Section: A Babel Of Other Designationsmentioning

confidence: 99%

Gustav Schimmelpenning and the Syndrome Bearing His Name

Happle

2004

Dermatology

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Gustav Schimmelpenning was born in 1928 in Oldenburg (Germany). From 1971 until 1994 he was head of the Department of Psychiatry at the University of Kiel. In 1957, while training in neurology and psychiatry, he comprehensively described a case of sebaceous nevus involving the head, with ipsilateral ocular lesions including coloboma of the upper lid, increased density of cranial bones, epileptic seizures and mental retardation. He concluded that this combination of anomalies represented a new ‘phacomatosis’. Subsequently this phenotype was reported by other authors under many different names, such as ‘Schimmelpenning syndrome’, ‘Feuerstein-Mims syndrome’, ‘Schimmelpenning-Feuerstein-Mims syndrome’, ‘epidermal nevus syndrome’, ‘Solomon syndrome’, ‘linear sebaceous nevus syndrome’, ‘organoid nevus phacomatosis’, or ‘Jadassohn nevus phacomatosis’. As a consequence of this confusing terminology, Schimmelpenning syndrome even has two different OMIM entries (no. 163200 and no. 165630). The term ‘Schimmelpenning syndrome’ is both historically justified and practically sufficient to distinguish this phenotype from other epidermal nevus syndromes.

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Sebaceous nevus syndrome: Report of two cases

Cited by 16 publications

References 7 publications

The group of epidermal nevus syndromes

The group of epidermal nevus syndromes

Encephalocraniocutaneous lipomatosis (Haberland syndrome) with bilateral cutaneous and visceral involvement

Gustav Schimmelpenning and the Syndrome Bearing His Name

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