Zobrazeno 1 - 10
of 45
pro vyhledávání: '"Pigmented Neurofibroma"'
Autor:
Juan A. Godínez-Chaparro, Adriana M. Valencia-Herrera, Carlos A. Mena-Cedillos, Sonia Toussaint-Caire, Mario R. Duarte-Abdala, Omar Loza-Escutia, Mirna E. Toledo-Bahena
Publikováno v:
Boletín Médico del Hospital Infantil de México, Vol 80, Iss 1 (2023)
Background: Pigmented (or melanocytic) neurofibroma (PN) constitutes only 1% of cases and is considered a rare variant of neurofibroma containing melanin-producing cells. In addition, the association of PN with hypertrichosis is infrequent. Case repo
Externí odkaz:
https://doaj.org/article/fbb67ae39ce74b6b831cf1b32c92dd11
Publikováno v:
GMS Interdisciplinary Plastic and Reconstructive Surgery DGPW, Vol 7, p Doc04 (2018)
Neurofibromatosis type 1 (NF1) is a tumor predisposition disease. Multiple neurofibromas are among the characteristic tumors of NF1. The report describes the diagnosis and treatment of a large spinal neurofibroma in a NF1 patient. The tumor showed a
Externí odkaz:
https://doaj.org/article/86e2704f16ca462d8a10d591246b394c
Publikováno v:
Indian Journal of Dermatology, Vol 60, Iss 1, Pp 46-50 (2015)
Neurotized congenital melanocytic nevus and pigmented neurofibroma (PNF) are close mimics and pose a clinicopathological challenge. We present a case of pigmented hypertrichotic plaque over lumbosacral region and discuss the differential diagnosis an
Externí odkaz:
https://doaj.org/article/1579e5600a39462980cdfec5ae4500c2
Publikováno v:
Archives of Medicine and Health Sciences, Vol 3, Iss 2, Pp 306-308 (2015)
Pigmented neurofibroma is a rare variant of neurofibroma commonly associated with neurofibromatosis 1 of diffuse type. Histopathologic examination is essential to differentiate it from other pigmented lesions. We report here a case of pigmented neuro
Externí odkaz:
https://doaj.org/article/c9139e6f9c484e5eb6c54644091741be
Akademický článek
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Publikováno v:
Archives of Medicine and Health Sciences, Vol 3, Iss 2, Pp 306-308 (2015)
Pigmented neurofibroma is a rare variant of neurofibroma commonly associated with neurofibromatosis 1 of diffuse type. Histopathologic examination is essential to differentiate it from other pigmented lesions. We report here a case of pigmented neuro
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::6dd95c9a0ff65d9e0834a761593cdfbf
http://www.amhsjournal.org/article.asp?issn=2321-4848
http://www.amhsjournal.org/article.asp?issn=2321-4848
Autor:
B. Efared, Hammas N, L. Chbani, Ebang Ga, Harmouch T, Hinde Elfatemi, Elousrouti Lt, Erreggad Fz, Sory I
Publikováno v:
Journal of Clinical Case Reports. 6
Introduction: Melanotic neurofibromas are rare tumours, derived from peripheral nerve sheath, whose originality consists in the presence of melanic pigment. The clinical and histological diagnosis is often difficult to make requiring the immunohistoc
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::7fefad20229ceae9ca4f9c962cd54aa5
https://doi.org/10.4172/2165-7920.1000804
https://doi.org/10.4172/2165-7920.1000804
Publikováno v:
Yonago Acta medica. 2007, 50(3), 65-68
Pigmented (melanotic) neurofibromas in the appendix are extremely rare. To our knowledge, this is the first case of appendiceal pigmented neurofibroma in a patient without neurofibromatosis 1, which was colonoscopically diagnosed. Histologically, the
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=dedup_wf_001::2e20bfada24201db81e29715dd8222fe
http://id.nii.ac.jp/1824/00005053/
http://id.nii.ac.jp/1824/00005053/
Publikováno v:
Histopathology. 20:527-530
We describe four cases of a distinctive myxoid change located in the centre of cellular blue naevi. Because all the reported lesions were large and were present on pressure-exposed locations, the myxoid change is thought to be caused by pressure toge
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::024ceaf0a9d62bcc0105671c78bc9a16
https://doi.org/10.1111/j.1365-2559.1992.tb01039.x
https://doi.org/10.1111/j.1365-2559.1992.tb01039.x
Autor:
Ito, Toshihiro
Publikováno v:
東京慈恵会医科大学雑誌. 117(4):277-284
article
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=jairo_______::27c88788cf738324e088be07db5d66df
https://ir.jikei.ac.jp/records/401
https://ir.jikei.ac.jp/records/401