Results 121 to 130 of about 67,419 (282)

Schwannomatosis of the Spinal Accessory Nerve: A Case Report. [PDF]

, 2019
Schwannomatosis is a distinct syndrome characterized by multiple peripheral nerve schwannomas that can be sporadic or familial in nature. Cases affecting the lower cranial nerves are infrequent.
Chin, Cynthia T, Jacques, Line, Lee, Anthony T, Lee, Young M, Morshed, Ramin A   +4 more
core  

Lithium Exposure Causes Trophoblast Cuproptosis by Upregulating FOXO1/STEAP4 Axis in Unexplained Miscarriage

Advanced Science, Volume 12, Issue 38, October 13, 2025.
Li exposure up‐regulates FOXO1 expression levels and thus promotes FOXO1‐mediated STEAP4 transcription, up‐regulating STEAP4 levels. Subsequently, STEAP4 up‐regulates intracellular Cu+ ion levels and causes cuproptosis, which further induces miscarriage.
Shuaishuai Xing, Yanbing Lin, Yi Sun, Xiaoping Yue, Qigang Fan, Jisheng Nie, Zhihong Zhang, Yajing Liu, Juntang Yang, Qingzheng Kang, Yanxin Wang, Haijun Yan, Chan Tian, Ying Chang, Huidong Zhang   +14 more
wiley   +1 more source

Primary Uterine Cervix Schwannoma: A Case Report and Review of the Literature

Case Reports in Pathology, 2012
Schwannoma (neurilemmoma) is a benign peripheral nerve sheath tumor that occurs in a wide variety of locations; however, its finding in the uterine cervix is extremely rare.
Maryam Tahmasbi, Johnny Nguyen, Masoumeh Ghayouri, Yuan Shan, Ardeshir Hakam   +4 more
doaj   +1 more source

An Unusual Case of Vulvar Schwannoma: A Case Report and Review of Literature [PDF]

Journal of Midwifery & Reproductive Health
Background & aim: Schwannoma seldom occurs in female genitalia; with only a few cases being reported in the medical literature. This tumor can present on labia majora, labia minora, clitoris, and vagina.
Asieh Maleki, Leila Pourali, Elahe Zandieh, Sara Mirzaeian   +3 more
doaj   +1 more source

An intra‐osseous tumour combination of biological importance—invasion of a melanotic schwannoma by an adamantinoma [PDF]

, 1961
J. J. Hodson
openalex   +1 more source

Severe Nerve Enlargement in SOS2‐Related Noonan Syndrome

American Journal of Medical Genetics Part A, Volume 197, Issue 10, October 2025.
ABSTRACT Noonan syndrome is a genetic multisystem congenital disorder, caused by pathogenic variants in genes that encode components of the RAS/MAPK signaling pathway. Pathogenic variants in SOS2 represent less than 2% of cases with NS. The phenotype includes a particularly high prevalence (65%) of lymphatic disease. Recently, severe nerve enlargements
Erika Leenders, Fieke Draaisma, Corrie E. Erasmus, Catelijne Coppens, Lotte E. R. Kleimeier, Melanie Burgers, Tuula Rinne, Martin Zenker, Laura Mazzanti, Wesley Reintjes, Nens van Alfen, Jos M. T. Draaisma   +11 more
wiley   +1 more source

Multicompartmental cystic trigeminal schwannoma as an uncommon differential diagnosis of cerebellopontine angle tumors

Radiology Case Reports
Trigeminal schwannoma is the second most common intracranial schwannoma yet accounts for less than 0.5% intracranial tumors [1]. Cystic degeneration is uncommon.
Yuen Hei Mak, MBBS(HK), FRCR, Grace Ho, MBChB(CUHK), FRCR, FHKCR, FHKAM(Radiology)   +1 more
doaj   +1 more source

Schwannoma of the Lower Leg with Malignant Transformation. A Case Report

European Journal of Case Reports in Internal Medicine, 2015
Background: Peripheral nerve sheath tumours are benign or malignant. Schwannoma is a benign peripheral nerve sheath tumour originating from Schwann cells that slowly grows eccentrically to the nerve axis. Malignant transformation of a schwannoma is rare.
Oana Serban, Laura Irina Poanta, Florin Mihaileanu, Daniela Fodor   +3 more
doaj   +1 more source

Granular cell myoblastoma—a misnomer. Electron microscopic and histochemical evidence concerning its schwann cell derivation and nature (granular cell schwannoma) [PDF]

, 1962
Edwin R. Fisher, Harry Wechsler
openalex   +1 more source

Ototoxicity in Cancer Therapies

Oral Diseases, EarlyView.
Sady Selaimen da Costa, Nathaniel S. Treister, Caio Eddie de Melo Alves   +2 more
wiley   +1 more source