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Soft tissue perineurioma and other unusual tumors in a patient with neurofibromatosis type 1.


ABSTRACT: Perineurioma is a rare benign peripheral nerve sheath tumor featuring perineurial differentiation. Perineurioma occurs sporadically with only one reported case in the setting of neurofibromatosis type 1 (NF-1). We present a 6.7-cm soft tissue perineurioma of the lower leg in a 51-year-old man with proven NF-1. The tumor displayed whorled and fascicular pattern with infiltrative margins and expressed EMA, GLUT-1, claudin-1, and CD34. Electron microscopy confirmed diagnosis. Furthermore, lipomatosis, cutaneous angiomatous nodules, vasculopathy, and iliac spine lesion consistent with non-ossifying fibroma were observed. Tumor DNA revealed no NF2 mutations or chromosomal aberrations but a germline NF1-deletion (c.449_502delTGTT) was detected in his blood sample. His brother displayed neurofibromas, duodenal ganglioneuroma and colonic juvenile polyp, and his mother a neurofibroma, cutaneous squamous cell carcinoma, and jejunal gastrointestinal stromal tumor (GIST); both were affected by NF-1. In conclusion, perineurioma may rarely be NF-1 related and should be included in the spectrum of neoplasms occurring in this disorder.

SUBMITTER: Schaefer IM 

PROVIDER: S-EPMC3843285 | biostudies-literature | 2013

REPOSITORIES: biostudies-literature

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Soft tissue perineurioma and other unusual tumors in a patient with neurofibromatosis type 1.

Schaefer Inga-Marie IM   Ströbel Philipp P   Thiha Aung A   Sohns Jan Martin JM   Mühlfeld Christian C   Küffer Stefan S   Felmerer Gunther G   Stepniewski Adam A   Pauli Silke S   Agaimy Abbas A  

International journal of clinical and experimental pathology 20131115 12


Perineurioma is a rare benign peripheral nerve sheath tumor featuring perineurial differentiation. Perineurioma occurs sporadically with only one reported case in the setting of neurofibromatosis type 1 (NF-1). We present a 6.7-cm soft tissue perineurioma of the lower leg in a 51-year-old man with proven NF-1. The tumor displayed whorled and fascicular pattern with infiltrative margins and expressed EMA, GLUT-1, claudin-1, and CD34. Electron microscopy confirmed diagnosis. Furthermore, lipomatos  ...[more]

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