Fibrolipomatous hamartoma of the nerve: a clinicopathologic report of 13 cases
Jazyk angličtina Země Spojené státy americké Médium print-electronic
Typ dokumentu časopisecké články
PubMed
24480457
DOI
10.1016/j.jaad.2013.10.002
PII: S0190-9622(13)01054-2
Knihovny.cz E-zdroje
- Klíčová slova
- Proteus syndrome, fibrolipomatous hamartoma of the nerve, macrodactyly, median nerve, syndactylia,
- MeSH
- dítě MeSH
- dospělí MeSH
- hamartom komplikace diagnóza patologie MeSH
- hodnocení rizik MeSH
- imunohistochemie MeSH
- jehlová biopsie MeSH
- lidé středního věku MeSH
- lidé MeSH
- lipom komplikace diagnóza patologie MeSH
- mladiství MeSH
- mladý dospělý MeSH
- nádory periferního nervového systému komplikace diagnóza patologie MeSH
- prognóza MeSH
- prsty ruky abnormality patologie MeSH
- vrozené deformity končetin etiologie patologie MeSH
- vzácné nemoci MeSH
- vzorkové studie MeSH
- Check Tag
- dítě MeSH
- dospělí MeSH
- lidé středního věku MeSH
- lidé MeSH
- mladiství MeSH
- mladý dospělý MeSH
- mužské pohlaví MeSH
- ženské pohlaví MeSH
- Publikační typ
- časopisecké články 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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