Results 81 to 90 of about 19,908 (210)
ALK Expression in Nerve Sheath Myxoma: A Potential Diagnostic Pitfall
Journal of Cutaneous Pathology, EarlyView.
Daniel Cole +6 more
wiley +1 more source
Clinical Case Reports, Volume 14, Issue 3, March 2026.Unravelling a Hidden Mass: Case of 70‐year‐old female presenting with 10‐year history of painless groin swelling. Intraoperative discovery revealed an unexpected neurofibroma. ABSTRACT This case presents the perplexing journey of a 70‐year‐old woman with a decade‐long history of painless, gradually enlarging left‐side groin swelling.
Alaa Tajeldeen Habeeb Abdallah +6 more
wiley +1 more source
Solitary neurofibroma of the inferior orbit: A rare occurrence
Muller Journal of Medical Sciences and Research, 2015 Solitary neurofibroma in the absence of neurofibromatosis is of rare occurrence and very few have been reported in the literature till now especially in the inferior orbit. A case of solitary neurofibroma of the inferior orbit is presented here.
V Sowmya +3 more
doaj +1 more source
Tailgut cyst and perineal hydatid cyst: A case report with multimodality imaging findings [PDF]
, 2016 A tailgut cyst is a rare developmental lesion and usually is located in the retrorectal or presacral space. Extrahepatic hydatid disease has been reported in several locations including the pelvis and it often poses a diagnostic challenge. There are very
Alghofaily, Khalefa Ali +3 more
core +4 more sources
Lymphangioma‐Induced Macroglossia in an Adolescent: A Case Report
Clinical Case Reports, Volume 14, Issue 3, March 2026.ABSTRACT Lymphangioma is a congenital malformation of the lymphatic system, commonly affecting the head and neck region. Macroglossia due to lymphangioma in adolescence is uncommon, making this case noteworthy. This condition can affect oral function, speech, and quality of life, making early diagnosis and intervention essential. This report highlights
Arezoo Heidary, Mojtaba Mehrabanian
wiley +1 more source
Children with 5′-end NF1 gene mutations are more likely to have glioma [PDF]
, 2017 Objective:To ascertain the relationship between the germline NF1 gene mutation and glioma development in patients with neurofibromatosis type 1 (NF1).Methods:The relationship between the type and location of the germline NF1 mutation and the presence of ...
Anastasaki, Corina +3 more
core +2 more sources
Intramuscular (infiltrating) Lipoma [PDF]
, 2011 Intraoral lipomas are benign and relatively rare tumors, although they occur with higher frequencies in other areas, most especially the back, abdomen and shoulders of adults.
Kashyap, Bina +2 more
core +1 more source
Cancer Reports, Volume 9, Issue 3, March 2026.ABSTRACT Background PRRX1‐rearranged mesenchymal neoplasms are rare soft tissue tumors with a predilection for the superficial subcutaneous tissue. The PRRX1::KMT2D fusion variant is exceptionally rare, with only three previously reported cases, all of which were located in the intermuscular regions.
Weixiang Zhong, Yu Deng, Ke Sun
wiley +1 more source
Chemokine receptor CCR3 is important for migration of mast cells in neurofibroma
Dermatologica Sinica, 2010 Background: Neurofibroma consists of abundant extracellular matrix and many types of cells, including Schwann cells (SCs), mast cells (MCs), fibroblasts and endothelial cells.
Wei-Chun Tai +4 more
doaj +1 more source
Schwannoma of the nasal septum-a case report [PDF]
, 2012 Schwannomas of the nasal cavity and paranasal sinuses are very rare. We report the case of a50-year-old woman with a schwannoma arising from the nasal septum.
Felix, Vinod +2 more
core +1 more source