Results 21 to 30 of about 12,175 (184)

The Solitary Variant of Mandibular Intraosseous Neurofibroma: Report of a Rare Entity

open access: yesCase Reports in Dentistry, 2015
Neurofibroma (NF) is a benign neoplasm derived from peripheral nerve cells. NF may extend either as a solitary lesion or as part of a generalized syndrome of neurofibromatosis.
Pavan Kumar Gujjar   +6 more
doaj   +1 more source

Cutaneous Neurofibroma of the Lacrimal Caruncule: A Case Report

open access: yesCase Reports in Ophthalmology, 2017
We describe the case of a neurofibroma on the lacrimal caruncle of a female patient with neurofibromatosis type 1 (NF1). NF1 is an autosomal dominant genetic disease with a wide variety of clinical manifestations, one of the most common of which is ...
Mario Motta, Mauro Geller, Cesar Motta
doaj   +1 more source

Pigmented neurofibroma with hypertrichosis

open access: yesBoletín Médico del Hospital Infantil de México, 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.
Juan A. Godínez-Chaparro   +6 more
doaj   +1 more source

Neurofibroma of the ovary [PDF]

open access: yesGynecologic Oncology, 1990
We report an unusual example of ovarian neurofibroma in a woman with neurofibromatosis (von Recklinghausen's disease). The neoplasm caused ovarian enlargement which surgically simulated malignant neoplasm. Ovarian neurofibromas are extremely rare and may arise from small myelinated nerves in the ovarian hilum.
Hegg, Cynthia A., Flint, Andrew
openaire   +3 more sources

Solitary Neurofibroma of the Frontal Sinus

open access: yesCase Reports in Otolaryngology, 2012
Isolated or solitary neurofibromas of the paranasal sinuses are rare. Mostly, they involve the maxillary sinus and so far, a solitary neurofibroma of the frontal sinus has never been reported in the literature.
Sudhir B. Sharma, Paul Hong
doaj   +1 more source

Neurofibroma Telinga Tengah dengan Otitis Media Supuratif Kronis

open access: yesJurnal Kesehatan Andalas, 2018
Pendahuluan: Neurofibroma adalah tumor saraf yang cukup sering dijumpai, tetapi hanya beberapa kasus yang melibatkan telinga tengah yang pernah dilaporkan.
Arsia Dilla Pramita   +2 more
doaj   +1 more source

Isolated Plexiform Neurofibroma of Arm with Unusual Presentation - A Rare Case Report [PDF]

open access: yesJournal of Clinical and Diagnostic Research, 2015
Plexiform neurofibroma (PNF) arises as a diffuse mass from nerve trunk and leads to overgrowth of cutis and subcutis structure. This is a case report of 20-year-old male, presented to our hospital with a giant ulcerated swelling over his left arm ...
PANKAJ KUMAR MISHRA   +3 more
doaj   +1 more source

Neurofibroma of the Colon: A Diagnostic Mimicker of Gastrointestinal Stromal Tumor

open access: yesCase Reports in Gastroenterology, 2016
Gastrointestinal neurofibroma usually develops as diffuse gastrointestinal involvement in neurofibromatosis type 1 patients. Only 4 cases of sporadic colonic neurofibroma in a patient without neurofibromatosis type 1 have been reported in the English ...
Soomin Ahn   +2 more
doaj   +1 more source

Solitary neurofibroma of the heart

open access: yesJournal of International Medical Research, 2020
Solitary neurofibroma of the heart is extremely unusual. Few reports of neurofibroma in the left ventricle have been published. In this case report, we present the results of transthoracic echocardiography, myocardial contrast echocardiography, cardiac ...
Pei Jing Li   +7 more
doaj   +1 more source

The 9th International RASopathies Symposium

open access: yesAmerican Journal of Medical Genetics Part A, EarlyView.
ABSTRACT The RASopathies are a group of congenital disorders with overlapping clinical manifestations that are caused by pathogenic germline or early somatic variants that result in the hyperactivation of the RAS/mitogen‐activated protein kinase (MAPK) signaling pathway.
Pau Castel   +41 more
wiley   +1 more source

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