Schimmelpenning syndrome

Linear nevus sebaceous syndrome-(a)Left hemimegalencephaly with agyria-pachygyria complex b)left ventricle colpocephaly

Schimmelpenning syndrome is a neurocutaneous condition characterized by one or more sebaceous nevi, usually appearing on the face or scalp,[1] associated with anomalies of the central nervous system, ocular system, skeletal system, cardiovascular system and genitourinary system.[2]

Synonyms include: "Linear nevus sebaceous syndrome (LNSS)", "Schimmelpenning-Feuerstein-Mims syndrome", "Feuerstein-Mims syndrome", "sebaceous nevus syndrome", "Solomon syndrome", and "Jadassohn's nevus phakomatosis". "Nevus" is sometimes spelled "naevus" and "sebaceous" may also be spelled "sebaceus". "Epidermal nevus syndrome" is sometimes used as a synonym, but more often as a broader term referring to Schimmelpenning syndrome in addition to nevus comedonicus syndrome, CHILD syndrome, Becker's nevus syndrome, and phakomatosis pigmentokeratotica.[3]

The classic Schimmelpenning syndrome diagnosis comprises a triad of sebaceous nevi, seizures, and mental retardation.[2] The condition was first reported by Gustav Schimmelpenning in 1957[4] and independently reported by Feuerstein and Mims in 1962.[5]

## Contents

* 1 Signs and symptoms
* 2 Genetic
* 3 Diagnosis
* 4 Management
* 5 Incidence
* 6 See also
* 7 References
* 8 External links

## Signs and symptoms[edit | edit source]

Since the original identification of Schimmelpenning syndrome, the number of findings has expanded to the point that the syndrome is associated with a considerable constellation of abnormalities.[2] The abnormalities may occur in a variety of combinations, and need not include all three aspects of the classic triad of sebaceous nevus, seizures and mental retardation[citation needed]. In 1998, a literature review by van de Warrenburg et al. found:

* seizures in 67% of cases
* mental retardation in 61% of cases
* ophthalmological abnormalities in 59% of cases
* involvement of other organ systems in 61% of cases
* structural abnormality of cerebrum or cranium in 72% of cases[6]

The major neurological abnormalities include mental retardation to varying extent, seizures, and hemiparesis.[7] Seizures, when present, typically begin during the first year of life.[8] The most common structural central nervous system abnormalities in Schimmelpenning syndrome are hemimegalencephaly and ipselateral gyral malformations.[3]

The major ocular abnormalities are colobomas and choristomas.[7]

Skeletal abnormalities may include dental irregularities, scoliosis, vitamin D-resistant rickets and hypophosphatemia. Cardiovascular abnormalities include ventricular septal defect and coarctation of the aorta; urinary system issues include horseshoe kidney and duplicated urinary collection system.[2]

## Genetic[edit | edit source]

Schimmelpenning syndrome appears to be sporadic rather than inherited, in almost all cases.[2] It is thought to result from genetic mosaicism, possibly an autosomal dominant mutation arising after conception and present only in a subpopulation of cells. The earlier in embryological development such a mutation occurs, the more extensive the nevi are likely to be and the greater the likelihood of other organ system involvement.[9]

## Diagnosis[edit | edit source]

The diagnosis of this condition is based on the following:[10]

* Characteristic signs/symptoms
* Medical history
* Biopsy
* X-ray (chest)

## Management[edit | edit source]

In general, children with a small isolated nevus and a normal physical exam do not need further testing;[9] treatment may include potential surgical removal of the nevus.[11] If syndrome issues are suspected, neurological, ocular, and skeletal exams are important. Laboratory investigations may include serum and urine calcium and phosphate, and possibly liver and renal function tests. The choice of imaging studies depends on the suspected abnormalities and might include skeletal survey, CT scan of the head, MRI, and/or EEG.[9]

Depending on the systems involved, an individual with Schimmelpenning syndrome may need to see an interdisciplinary team of specialists: dermatologist, neurologist, ophthalmologist, orthopedic surgeon, oral surgeon, plastic surgeon, psychologist.[9]

## Incidence[edit | edit source]

Nevus sebaceous was first identified in 1895 by Jadassohn.[12] Sebaceous nevi occur in 1 to 3 of 1000 births, with equal incidence by sex.[3] There is no test to determine whether an individual born with a sebaceous nevus will go on to develop further symptoms of Schimmelpenning syndrome. It has been reported that up to 10% of individuals with epidermal nevi may develop additional syndrome symptoms,[3] but that number appears to be inconsistent with the rarity of the syndrome and may be overstated.[13] Prevalence is unknown, but Epidermal nevus syndrome is listed with the National Organization for Rare Disorders, which defines rare as affecting "fewer than 200,000 people in the United States."[14]

## See also[edit | edit source]

* Epidermis
* Epidermal nevus syndrome
* Skin lesion
* List of cutaneous conditions

## References[edit | edit source]

1. ↑ Menascu, Shay; Donner, Elizabeth J. (2008). "Linear nevus sebaceous syndrome: case reports and review of the literature". Pediatric Neurology. 38 (3): 207–10. doi:10.1016/j.pediatrneurol.2007.10.012. ISSN 0887-8994. PMID 18279757.
2. ↑ 2.0 2.1 2.2 2.3 2.4 Eisen, D.B.; Michael, D.J. (2009). "Sebaceous lesions and their associated syndromes: Part II". Journal of the American Academy of Dermatology. 61 (4): 563–78. doi:10.1016/j.jaad.2009.04.059. ISSN 0190-9622. PMID 19751880.
3. ↑ 3.0 3.1 3.2 3.3 Burns, Tony, ed. (2004). Rook's Textbook of Dermatology (7th ed.). Malden, Mass.: Blackwell Science. ISBN 0-632-06429-3.
4. ↑ Schimmelpenning, G. (1957). "Klinischer Beitrag zur Symptomatology der Phacomatosen". Fortschr Röntgenstr. 87 (6): 716–20. doi:10.1055/s-0029-1213358. PMID 13512450.
5. ↑ Feuerstein, RC; Mims, LC (1962). "Linear nevus sebaceus with convulsions and mental retardation". Am. J. Dis. Child. 104 (6): 674–679. doi:10.1001/archpedi.1962.02080030675013. PMID 13944982.
6. ↑ van de Warrenburg BP, van Gulik S, Renier WO, Lammens M, Doelman JC (1998). "The linear naevus sebaceus syndrome". Clinical Neurology and Neurosurgery. 100 (2): 126–132. doi:10.1016/S0303-8467(98)00012-2. PMID 9746301.
7. ↑ 7.0 7.1 Harper, J.; A.P. Oranje; N.S. Prose (2006). Textbook of Pediatric Dermatology. Malden, Mass.: Blackwell.
8. ↑ Lovejoy FH Jr, Boyle WE Jr (1973). "nevus sebaceous syndrome: Report of two cases and a review of the literature". Pediatrics. 52 (3): 382–7. PMID 4730395.`{{cite journal}}`: CS1 maint: uses authors parameter (link)
9. ↑ 9.0 9.1 9.2 9.3 Roach, E. Steve, ed. (2004). Neurocutaneous Disorders. Cambridge, UK: Cambridge University Press. pp. 88–104. ISBN 0-521-78153-1.
10. ↑ "Nevus Sebaceus Syndrome". NORD (National Organization for Rare Disorders). Archived from the original on 21 March 2021. Retrieved 9 April 2022.
11. ↑ Eisen, DB; DJ Michael (2009). "Sebaceous lesions and their associated syndromes: Part I". J Am Acad Dermatol. 61 (4): 549–60. doi:10.1016/j.jaad.2009.04.058. PMID 19751879.
12. ↑ Jadassohn, J. (1895). "Bemerkungen zur Histologie der systematisirten Naevi und ueber 'Talgdruesen-naevi'". Archiv für Dermatologie und Syphilis. 33: 355–372. doi:10.1007/BF01842810. Archived from the original on 2022-04-11. Retrieved 2021-08-11.
13. ↑ "LNSS Connections: About Linear Nevus Sebaceous Syndrome". 2010-04-13. Archived from the original on 2010-03-16. Retrieved 2010-04-15.
14. ↑ "Disease Information from NORD, National Organization of Rare Diseases, Inc". 2010-01-20. Archived from the original on 2010-07-04. Retrieved 2010-04-15.

## External links[edit | edit source]

Classification|

* ICD-10: Q85.8
* OMIM: 163200

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External resources|

* Orphanet: 2612