Results 111 to 120 of about 67,419 (282)
Extradural cervical spinal schwannoma in a child: a case report and review of the literature
Introduction Extradural schwannoma arising from high cervical spinal root is a rare entity in children. We report a case of extradural cervical schwannoma in a 14-year-old boy.
Apar Pokharel +5 more
doaj +1 more source
Abstract Background The normal tissue objective (NTO) is an inverse planning approach in radiosurgery, also available for the CyberKnife system. By employing a model function, it aims to achieve precise control over the global dose fall‐off in healthy tissue.
Nadine Sonntag +6 more
wiley +1 more source
Plexiform schwannoma of the floor of the mouth: a case report
Plexiform schwannoma is a type of schwannoma that can be occured at any age and any site of the oral cavity. In the gross and histopathological features, it shows plexiform or multinodular growth pattern.
Mohammad Koochek Dezfuli +4 more
doaj
Abdominal Wall Schwannoma: A Rare Case of Target Sign on Ultrasonography
The target sign observed on ultrasonography. ABSTRACT Schwannoma is a benign tumor derived from Schwann cells of peripheral nerves. Schwannomas arising within muscle or fat exhibit characteristic magnetic resonance imaging (MRI) findings called the target sign, split fat sign, or fascicular sign.
Noboru Takanashi +8 more
wiley +1 more source
A rare case of schwannoma: schwannoma of the tongue
Schwannomas, also known as the neurolemmomas, are caused by the Schwann cells in the peripheral, cranial or autonomic nerve sheath. These are benign, solid and encapsulated tumors. They grow slowly. Generally they are seen between the ages of 20-50 years old and they are more common in females than males, F / M :1,5-2 / 1.
YILMAZ, Hasan +2 more
openaire +3 more sources
The molecular pathogenesis of schwannomatosis, a paradigm for the co-involvement of multiple tumour suppressor genes in tumorigenesis [PDF]
Schwannomatosis is characterized by the predisposition to develop multiple schwannomas and, less commonly, meningiomas. Despite the clinical overlap with neurofibromatosis type 2 (NF2), schwannomatosis is not caused by germline NF2 gene mutations ...
Cooper, David Neil +3 more
core +1 more source
ABSTRACT Solitary fibrous tumors (SFTs) are rare neoplasms characterized by spindle neoplastic cell proliferation within collagenous stroma and prominent dilated vasculature. They present a wide histopathological spectrum, ranging from hypocellular lesions with a rich collagenous stroma to hypercellular lesions with scant stroma.
Hiroyuki Okanishi +10 more
wiley +1 more source
Giant Vulvar Schwannoma: A Case Report
Schwannoma is a solitary, slow growing, benign tumour of the peripheral nerve sheath, and it is most common locations are the head, neck, the flexor surfaces of the extremities, retroperitoneal and posterior mediastinium. External female genital organs
Murat Bozkurt, Duygu Kara
doaj +2 more sources
A unique case of epithelioid schwannoma; rare soft tissue tumor
Epithelioid schwannoma is a rare histological subtype of schwannoma that can cause diagnostic challenges. Most reported cases in the literature were located predominantly in the dermis and subcutaneous tissue of the extremities and trunk.
Haneen Al-Maghrabi, Njoud Aldardeir
doaj +1 more source
We describe an unusual case of cervical meningioma presenting as a carotid body tumour. This case emphasises the importance of cytoradiologic correlation in lesions with atypical imaging findings; and the crucial role of fine needle aspiration cytology in accurately diagnosing masses in precarious anatomic sites of the head and neck.
Poorva Singh +3 more
wiley +1 more source

