Zobrazeno 1 - 10
of 450
pro vyhledávání: '"Primary pulmonary lymphoma"'
Publikováno v:
Global Journal of Medicine and Public Health, Vol 4, Iss 6 (2024)
A 55-year-old female presented with history of fever, dry cough and right sided chest pain of two months duration. Radiological examination revealed a soft tissue attenuated lesion involving right middle lobe. Immuno histochemical analysis lead
Externí odkaz:
https://doaj.org/article/ac0f728d185b47c7b572f3d4b8fc9416
Autor:
Kajetan Kiełbowski, Dawid Kordykiewicz, Janusz Jesionka, Janusz Wójcik, Konrad Ptaszyński, Konstantinos Kostopanagiotou, Piotr Waloszczyk, Małgorzata Edyta Wojtyś
Publikováno v:
Medicina, Vol 60, Iss 6, p 840 (2024)
Primary pulmonary lymphoma is a rare neoplasm characterized by the proliferation of lymphoid tissue affecting the lungs. The most common subtype is marginal zone lymphoma of mucosa-associated lymphoid tissue (MALT). Rarely, a MALT lymphoma transforms
Externí odkaz:
https://doaj.org/article/c44b513754e8431cbb96a1a0ab7e7938
Autor:
Yasuhito Sekimoto, Mitsuaki Sekiya, Makiko Kohmaru, Tomoko Okuma, Manabu Tajima, Hideaki Sato, Kazuhisa Takahashi
Publikováno v:
Respirology Case Reports, Vol 11, Iss 7, Pp n/a-n/a (2023)
Key message Ultrasound‐guided transthoracic needle biopsy is a relatively safe procedure diagnosing subpleural pulmonary mass and has high sensitivity in the diagnosis of lung cancer. However, the usefulness in other rare malignancies is unknown. T
Externí odkaz:
https://doaj.org/article/876c6e41121c4a35bdb23b2f7b4a4c18
Autor:
Nobuhiro Fujioka, Yoshiro Kai, Ryosuke Kataoka, Kentaro Suzuki, Kazuhiro Sakaguchi, Yoshifumi Yamamoto, Takeshi Kawaguchi, Noriyoshi Sawabata, Haruyuki Tanaka, Minami Matsuoka, Maiko Takeda, Shigeo Muro
Publikováno v:
Respirology Case Reports, Vol 11, Iss 3, Pp n/a-n/a (2023)
Abstract Primary pulmonary diffuse large B‐cell lymphoma is a rare entity. We describe a case of pulmonary lymphoma with multiple nodules mimicking metastases in a treated patient with rheumatoid arthritis. A 73‐year‐old man was diagnosed with
Externí odkaz:
https://doaj.org/article/b04eb946e11348428f172d0960850c58
Autor:
Zhiwei Peng, Li Yi, Yahong Tao, Zhiyong Chen, Ze Lin, Anjing He, Mengni Jin, Fanrong Liu, Minjing Zuo
Publikováno v:
Frontiers in Oncology, Vol 12 (2022)
BackgroundThe risk of gastrointestinal stromal tumor (GIST) in combination with other primary malignancies is high, which occurs before and after the diagnosis of GIST. Primary pulmonary T-cell lymphoma is a rare type of non-Hodgkin lymphoma.Case pre
Externí odkaz:
https://doaj.org/article/fb129e503d1046b89c7f30c8631b928b
Publikováno v:
Frontiers in Oncology, Vol 12 (2022)
BackgroundThe occurrence of primary pulmonary lymphoma (PPL) as a secondary malignancy in patients diagnosed with chronic myeloid leukemia (CML) is extremely rare. As the clinical manifestations are atypical, most patients with PPL tend to be misdiag
Externí odkaz:
https://doaj.org/article/cc46d8737c034c79886feb1e1878929c
Autor:
Ying Peng, Wanling Qi, Zhehuang Luo, Qingyun Zeng, Yujuan Huang, Yulu Wang, Amit Sharma, Ingo G. H. Schmidt-Wolf, Fengxiang Liao
Publikováno v:
Frontiers in Oncology, Vol 12 (2022)
BackgroundPrimary pulmonary lymphoma (PPL) is defined as clonal abnormal hyperplasia of lung parenchyma or bronchial lymphoid tissue originating from bronchial mucosal tissue. However, PPL is rare, which accounts for approximately 3-4% of extraneurot
Externí odkaz:
https://doaj.org/article/012cd5f458c64dd5b3b8543d6d0c73d5
Publikováno v:
Frontiers in Oncology, Vol 12 (2022)
BackgroundTo date, there is no treatment consensus on mucosa-associated lymphoid tissue (MALT) derived primary pulmonary lymphoma (PPL).MethodsWe identified patients with early-stage MALT-type PPL from the National Cancer Institute’s Surveillance,
Externí odkaz:
https://doaj.org/article/b2771838f3104d60b97decdb1aa450da
Akademický článek
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Autor:
Hui Shen, Yaodong Zhou
Publikováno v:
Frontiers in Oncology, Vol 12 (2022)
BackgroundPrimary pulmonary lymphoma (PPL) is a rare clonal lymphoproliferative lung disease. The present study analyzes the clinical features, imaging data, pathologic characteristics, treatment, and prognosis of PPL patients, with the aim to discus
Externí odkaz:
https://doaj.org/article/80b5bc13f2f14af79a4363587e2e5df9