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A case of endobronchial mucosa-associated lymphoid tissue (MALT) lymphoma successfully treated with radiotherapy and a review of the literature.
Arai, Rino; Tanifuji, Mizuka; Nagai, Asuka; Ebihara, Akinori; Iwamoto, Tokuzen; Onaka, Shinnosuke; Aoyama, Mayumi; Otaki, Makoto; Shigemitsu, Hidenobu; Kuwahira, Ichiro.
Afiliación
  • Arai R; Respiratory Disease Center Tokyo General Hospital Tokyo Japan.
  • Tanifuji M; Department of Diagnostic Imaging and Nuclear Medicine Tokyo Women's Medical University Tokyo Japan.
  • Nagai A; Department of Respiratory Medicine Niigata University School of Medicine Niigata Japan.
  • Ebihara A; Department of Pulmonary Medicine Tokai University Tokyo Hospital Tokyo Japan.
  • Iwamoto T; Department of Pulmonary Medicine Tokai University Tokyo Hospital Tokyo Japan.
  • Onaka S; Respiratory Disease Center Tokyo General Hospital Tokyo Japan.
  • Aoyama M; Respiratory Disease Center Tokyo General Hospital Tokyo Japan.
  • Otaki M; Midtown Clinic Medical Corporation Himedic Yamanakako Yamanashi Japan.
  • Shigemitsu H; Department of Critical Care Medicine St. Rose Dominican Siena Hospital Las Vegas Nevada USA.
  • Kuwahira I; Respiratory Disease Center Tokyo General Hospital Tokyo Japan.
Respirol Case Rep ; 12(5): e01369, 2024 May.
Article en En | MEDLINE | ID: mdl-38721113
ABSTRACT
A 60-year-old man was noted to have an elevated lesion in the right mainstem bronchus on chest computed tomography (CT) during his annual medical checkup 3 years previously. The lesion had gradually increased in size. FDG-PET showed no accumulation. Bronchoscopy revealed 5 nodular smooth surface protrusions on the ventral surface of the right mainstem bronchus, with the largest lesion that measured 5 mm in diameter. Biopsy showed diffuse infiltration of small lymphocytes, positive for CD20 and subsequently diagnosed with mucosa-associated lymphoid tissue (MALT) lymphoma. The lesions disappeared on chest CT after radiotherapy, and no recurrence has been observed after 5 years. We reviewed 48 cases of endobronchial MALT lymphoma in the literature and provided a comprehensive review of the literature to date including our case.
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Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Idioma: En Revista: Respirol Case Rep Año: 2024 Tipo del documento: Article

Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Idioma: En Revista: Respirol Case Rep Año: 2024 Tipo del documento: Article
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