Neurofibromatosis type 1

Neurofibromatosis type 1 (NF1) is a clinically heterogeneous, neurocutaneous genetic disorder characterized by café-au-lait spots, iris Lisch nodules, axillary and inguinal freckling, and multiple neurofibromas.

Subcutaneous neurofibromas

The presence of Neurofibromas in the subcutis.


Total: 3

                       


(per page)
PMID (PMCID)
25672557
 FEMALE Adult
[A case of ganglioglioma extended to the lateral ventricle and associated with neurofibromatosis type 1].
Enomoto T, Fukushima Y, Yoshino S, Hirakawa K, Fukushima T, Aoki M, Nabeshima K, Tsugu H, Inoue T.
No Shinkei Geka. 2015;43(2):147-52.
She was diagnosed with neurofibromatosis type 1 because she had multiple subcutaneous neurofibromas and cafe au lait spots.
22317879
 FEMALE Middle Aged
Neurofibroma of the cervix presenting as cervical stenosis in a patient with neurofibromatosis type 1: a case report.
Lastra RR, Bavuso N, Randall TC, Brooks JS, Barroeta JE.
Int J Gynecol Pathol. 2012;31(2):192-194.
Neurofibromatosis type 1 is an autosomal dominant disorder characterized by the presence of cutaneous and subcutaneous neurofibromas as well as deep-seated plexiform neurofibromas.
2517814
 MALE Adult
Neurofibromatosis type 1 with bilateral acoustic neuromas.
Michels VV, Whisnant JP, Garrity JA, Miller GM.
Neurofibromatosis. 1989;2(4):213-7.
A patient diagnosed as having neurofibromatosis type 1 (NF-1) on the basis of 6 cafe-au-lait macules, multiple subcutaneous neurofibromas and 1 Lisch nodule is described.