Bilateral pulmonary nodules in a patient with extensive autoimmune disease

[...]surgical thoracoscopy was performed with wedge resection. The disease has no specific signs and symptoms; 36% of patients are asymptomatic at diagnosis.2 Radiographic imaging shows variable presentation.3 Diagnosis requires a surgical biopsy, usually wedge resection, during video-assisted thora...

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Veröffentlicht in:Thorax 2019-11, Vol.74 (11), p.1089-1090
Hauptverfasser: Patel, Sachin, Nasser, Wael, Khan, Rumi, Herrera, Luis
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container_end_page 1090
container_issue 11
container_start_page 1089
container_title Thorax
container_volume 74
creator Patel, Sachin
Nasser, Wael
Khan, Rumi
Herrera, Luis
description [...]surgical thoracoscopy was performed with wedge resection. The disease has no specific signs and symptoms; 36% of patients are asymptomatic at diagnosis.2 Radiographic imaging shows variable presentation.3 Diagnosis requires a surgical biopsy, usually wedge resection, during video-assisted thoracoscopy or thoracotomy, as the yield from bronchoscopic transbronchial and CT-guided biopsies is very low.4 Immunohistochemical staining is crucial to assess the architecture of the lymphoid infiltrate and to exclude other lymphomas.1 Pulmonary MALT lymphoma has an excellent 5-year overall survival rate (>80%). Contributors SP, the principal author, made substantial contributions to study conception and design, acquisition, analysis and interpretation of data, and drafting and final revision of the manuscript.
doi_str_mv 10.1136/thoraxjnl-2019-213632
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The disease has no specific signs and symptoms; 36% of patients are asymptomatic at diagnosis.2 Radiographic imaging shows variable presentation.3 Diagnosis requires a surgical biopsy, usually wedge resection, during video-assisted thoracoscopy or thoracotomy, as the yield from bronchoscopic transbronchial and CT-guided biopsies is very low.4 Immunohistochemical staining is crucial to assess the architecture of the lymphoid infiltrate and to exclude other lymphomas.1 Pulmonary MALT lymphoma has an excellent 5-year overall survival rate (&gt;80%). 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The disease has no specific signs and symptoms; 36% of patients are asymptomatic at diagnosis.2 Radiographic imaging shows variable presentation.3 Diagnosis requires a surgical biopsy, usually wedge resection, during video-assisted thoracoscopy or thoracotomy, as the yield from bronchoscopic transbronchial and CT-guided biopsies is very low.4 Immunohistochemical staining is crucial to assess the architecture of the lymphoid infiltrate and to exclude other lymphomas.1 Pulmonary MALT lymphoma has an excellent 5-year overall survival rate (&gt;80%). 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subjects Arthritis
Autoimmune diseases
Autoimmune Diseases - complications
bronchial-associated lymphoid tissue
Chest clinic
Family medical history
Female
Humans
Image-Guided Biopsy
Immunoglobulins
Incidental Findings
Lung Neoplasms - complications
Lung Neoplasms - diagnosis
Lung Neoplasms - pathology
Lung Neoplasms - surgery
Lymphoma
Lymphoma, B-Cell, Marginal Zone - complications
Lymphoma, B-Cell, Marginal Zone - diagnosis
Lymphoma, B-Cell, Marginal Zone - pathology
Lymphoma, B-Cell, Marginal Zone - surgery
MALT lymphoma
Microscopy
Middle Aged
mucosa-associated lymphoid tissue (MALT)
Multiple Pulmonary Nodules - complications
Multiple Pulmonary Nodules - diagnosis
Multiple Pulmonary Nodules - pathology
Multiple Pulmonary Nodules - surgery
Ostomy
Pathogenesis
Positron-Emission Tomography
pulmonary lymphoma
Radiography, Thoracic
Sjrogren’s syndrome
Tomography, X-Ray Computed
title Bilateral pulmonary nodules in a patient with extensive autoimmune disease
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