Significats de rare neoplasm en anglès

Schwannoma originating from the cervical vagus nerve is an extremely rare neoplasm.

Conclusions: Non-keratinizing squamous cell carcinoma is a rare neoplasm with distinct morphological characteristics.

The intra-abdominal desmoplastic small round cell tumor is a rare neoplasm.

Skull base chordomas are a rare neoplasm arising from the notochord.

Solitary fibrous tumor is a rare neoplasm of mesenchymal origin that usually affects the pleura.

Conclusion: Solid pseudopapillary tumor of the pancreas is a rare neoplasm usually found in young women.

The incidence, the characteristic features, the histogenesis, and the anatomical pathology of this rare neoplasm are mentioned.

Primary malignant melanoma (MM) of the uterine cervix is an extremely rare neoplasm, with about 78 cases described in the literature.

Introduction: Mucinous adenocarcinoma is a rare neoplasm of the gastrointestinal tract and one of the three major histological subtypes of the primary appendiceal adenocarcinoma.

Primary carcinoid of the testis is an extremely rare neoplasm, making up 0.23% of all testicular neoplasms.

Thyroid carcinoma showing thymic-like differentiation (CASTLE) comprises a rare neoplasm of the thyroid gland which arises from ectopic thymic tissue or remnants of brachial pouches.

Olfactory neuroblastoma (ONB) is a rare neoplasm of the head and neck region that is included in the differential diagnosis of other sinonasal tract malignancies.

Objective: Cervical sarcomas are exceedingly rare neoplasms associated with a poor prognosis.

Intraspinal PNETs are rare neoplasms that are usually metastatic in origin.

Extracranial schwannomas in the head and neck region are rare neoplasms.

Childhood brain tumors (CBT) include a diversity of rare neoplasms of largely unknown etiology.