Results 21 to 30 of about 338,057 (225)

A thymoma or not a thymoma—that is the question: a case report

open access: yesMediastinum, 2021
Thymomas are malignant, epithelial tumors of the thymus of diverse morphology that may metastasize or relapse after resection. The WHO histological classification includes five main subtypes A, AB, B1, B2 and B3. Types A and AB usually harbour a specific GTF2I gene mutation.
Szolkowska, Malgorzata   +8 more
openaire   +2 more sources

Congenital thymoma [PDF]

open access: yesAutopsy Case Reports, 2021
Thymomas are a heterogeneous group of tumors arising from the epithelium of the thymus. They are categorized by the proportion of neoplastic epithelia to lymphocytes and by the degree of cytologic atypia. Thymomas constitute 0.2-1.5% of all malignancies and nearly all occur in patients over 20 years.
Chand, Momal Tara   +4 more
openaire   +4 more sources

When to suspect a thymoma: clinical point of view. [PDF]

open access: yes, 2020
The thymus plays a crucial role in the development of immune system, regulating the maturation, selection and migration of T lymphocytes. Alterations in lymphatic content and structure of the thymus are observed in many autoimmune diseases.
Kocher, Gregor J.   +3 more
core   +2 more sources

Thymoma and cancer [PDF]

open access: yesCancer, 1968
Twenty-one per cent (31 of 146) of patients who had thymoma and whose condition was followed for 20 years had a malignant lesion of a nonthymic tissue. In contrast, 8% (15 of 177) of patients who had a parathyroid adenoma had a malignant neoplasm of another tissue.
J V, Souadjian   +2 more
openaire   +2 more sources

Viral infection in thymoma and thymic tumors with autoimmune diseases

open access: yesThoracic Cancer, 2021
A thymoma is a type of thymic tumor which is rarely malignant that is frequently reported in adult patients. A number of thymoma‐related immune disorders are observed including autoimmune diseases, which suggests a strong connection between thymoma ...
Rui Chang   +3 more
doaj   +1 more source

Type B3 thymoma associated membranous nephropathy: A rare case and review of the literature

open access: yesHuman Pathology: Case Reports, 2021
Thymoma can cause several autoimmune conditions in a number of patients. Nephrotic syndrome is considered to be a rare systemic manifestation from thymic lesions.
Sakda Sathirareuangchai   +3 more
doaj   +1 more source

Real‐world study of treatment and outcome of type B2 + B3 thymoma: The neglected part of thymoma

open access: yesThoracic Cancer, 2023
Background This study aimed to examine the treatment and prognosis of patients with type B2 + B3 thymoma and compare it with those patients with type B2 and B3 thymoma. Methods We conducted a retrospective analysis of the results of 39 patients with type
Ke Zhao   +13 more
doaj   +1 more source

Thymoma-Related Paraneoplastic Syndrome Mimicking Reactive Arthritis

open access: yesMedicina, 2021
Background and Objectives: Thymomas are associated with a high frequency of paraneoplastic manifestations. Paraneoplastic syndrome (PNS) with thymoma presents a challenge to clinicians because of the need to decipher the association between the ...
Chang-Hung Liao   +4 more
doaj   +1 more source

Sclerosing thymoma-like thymic amyloidoma with nephrotic syndrome: a case report

open access: yesJournal of Medical Case Reports, 2017
Background Primary localized amyloidosis presenting as an isolated mediastinal mass is extremely rare, especially in the thymus. Sclerosing thymoma is also an extremely rare anterior mediastinal tumor, pathologically characterized by extensive sclerotic ...
Yuto Kato   +8 more
doaj   +1 more source

Correlation of Prognostic Nutritional Index with Overall Survival of Postoperative Patients with Thymoma

open access: yesZhongliu Fangzhi Yanjiu, 2021
Objective To evaluate the correlation of prognostic nutritional index(PNI) with overall survival of postoperative patients with thymoma. Methods The clinical and pathological data of 173 postoperative patients with thymoma were analyzed retrospectively ...
WANG Yan   +3 more
doaj   +1 more source

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