Fibrolipomatous hamartoma of the nerve: a clinicopathologic report of 13 cases
Language English Country United States Media print-electronic
Document type Journal Article
PubMed
24480457
DOI
10.1016/j.jaad.2013.10.002
PII: S0190-9622(13)01054-2
Knihovny.cz E-resources
- Keywords
- Proteus syndrome, fibrolipomatous hamartoma of the nerve, macrodactyly, median nerve, syndactylia,
- MeSH
- Child MeSH
- Adult MeSH
- Hamartoma complications diagnosis pathology MeSH
- Risk Assessment MeSH
- Immunohistochemistry MeSH
- Biopsy, Needle MeSH
- Middle Aged MeSH
- Humans MeSH
- Lipoma complications diagnosis pathology MeSH
- Adolescent MeSH
- Young Adult MeSH
- Peripheral Nervous System Neoplasms complications diagnosis pathology MeSH
- Prognosis MeSH
- Fingers abnormalities pathology MeSH
- Limb Deformities, Congenital etiology pathology MeSH
- Rare Diseases MeSH
- Sampling Studies MeSH
- Check Tag
- Child MeSH
- Adult MeSH
- Middle Aged MeSH
- Humans MeSH
- Adolescent MeSH
- Young Adult MeSH
- Male MeSH
- Female MeSH
- Publication type
- Journal Article MeSH
BACKGROUND: Fibrolipomatous hamartoma of the nerve is a rare benign infiltrating condition of peripheral nerves with prominent cutaneous findings that has not being well described in the dermatologic and dermatopathologic literature. OBJECTIVE: We sought to evaluate the clinical and histopathological features of this rare condition. METHODS: We reviewed the clinicopathologic features of 13 cases to delineate their clinical presentation and histopathologic spectrum. RESULTS: All patients presented with unilateral lesions on the thenar areas, fingers, or both. In 7 cases the lesions presented congenitally and in 6 cases the lesions presented sporadically. Histologically, we found 2 patterns that have only been rarely mentioned before including cases with intraneural perineurioma-like features and cases with marked nerve hyperplasia. LIMITATIONS: Only 13 cases were included in our study. CONCLUSIONS: This condition is an uncommon entity. The diagnosis of this disorder can be highly suspected on its macroscopic features. Predilection of the median nerve and the frequent association with macrodactyly are characteristic clinical findings.
Department of Dermatology Universidad Autonoma de Madrid Fundacion Jimenez Diaz Madrid Spain
Department of Hand Surgery and Plastic Surgery Vysoke nad Jizerou Czech Republic
Department of Pathology and Dermatology Hospital Obrero La Paz Bolivia
Hospital Aleman Buenos Aires Argentina
Instituto Valenciano de Oncologia Valencia Spain
Sikls's Department of Pathology Charles University Medical Faculty Hospital Pilsen Czech Republic
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