Pulmonary mucosa-associated lymphoid tissue lymphoma revisited

Borie, Raphaël; Wislez, Marie; Antoine, Martine; Copie‐Bergman, Christiane; Thiéblemont, Catherine; Cadranel, Jacquès

doi:10.1183/13993003.01701-2015

Cited by 68 publications

(120 citation statements)

References 96 publications

(155 reference statements)

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“…Two patients (10%) had autoimmune disease. These results were similar to those for PML (1,3). The location of the tumor in 14 patients (70%) was the central airway, and 4 patients (20%) had lobar atelectasis.…”

Section: Discussionsupporting

confidence: 88%

“…Gelder et al reviewed 321 primary tracheal tumors and reported that 54.2% were squamous cell carcinoma (SCC), 10.6% were adenoid cystic carcinoma (ACC), and only 4 out of 321 (1.2%) were lymphoma (2). Bronchus-associated lymphoid tissue (BALT) can be found in follicular bronchiolitis and can be associated with various autoimmune disorders, such as Sjögren's syndrome, but is not found in the normal lung (1). When a primary PML develops from BALT, it is known as BALT lymphoma.…”

Section: Discussionmentioning

confidence: 99%

“…PPL represents only 0.5-1% of lung neoplasia cases, and most of these are extranodal marginal zone B-cell lymphoma of mucosa-associated lymphoid tissue (MALT lymphoma) (1). The presence of an immune system disorder was identified as a predisposing factor for the development of pulmonary MALT lymphoma (PML), and its distinctive computed tomography (CT) findings are associated with bilateral/multiple lesions and air bronchogram.…”

Section: Introductionmentioning

confidence: 99%

See 2 more Smart Citations

Endobronchial Mucosa-associated Lymphoid Tissue Lymphoma: A Report of Two Cases and a Review of the Literature

et al. 2018

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Primary endobronchial mucosa-associated lymphoid tissue lymphoma (EML) is rare. We reviewed 20 cases of EML, including ours and case reports. We found that the location of tumor in 70% of these cases was limited to the trachea and main bronchus, and the form of tumor in 61% of these cases was several nodular protrusions. If a patient exhibits these characteristics, adequate specimen collection on bronchoscopy is important. Because the prognosis for patients with EML is good, tumors on the trachea and main bronchus should be treated, while those on the peripheral airway can be watched carefully.

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Section: Discussionsupporting

confidence: 88%

Section: Discussionmentioning

confidence: 99%

Section: Introductionmentioning

confidence: 99%

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Endobronchial Mucosa-associated Lymphoid Tissue Lymphoma: A Report of Two Cases and a Review of the Literature

et al. 2018

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“…NPA has been reported to mask underlying malignancies in a few case reports including haematological malignancies and, rarely, mucosal-associated lymphoid tissue (MALT) lymphoma 9. Often, NPA can be completely asymptomatic and may be diagnosed as an incidentaloma on chest imaging.…”

Section: Introductionmentioning

confidence: 99%

Nodular pulmonary amyloidosis: a complex disease with malignancy association

Core

Alsaad²,

Jiang

et al. 2017

BMJ Case Reports

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Pulmonary amyloidosis is a rare disease that incorporates deposition of amyloid microfibril material in the lung parenchyma. The condition generally presents as an indolent subacute-to-chronic pulmonary disease and requires tissue biopsy to establish the diagnosis. Nodular pulmonary amyloidosis, a subtype of pulmonary amyloidosis, is characterised by special radiographic and pathological features. While the disease can be associated with inflammatory conditions; its association with mucosal-associated lymphoid tissue (MALT lymphoma) is unusual and carries management challenges. Herein, we illustrate a case study of nodular pulmonary amyloidosis associated with underlying MALT lymphoma in a patient with known systemic lupus erythematosus. The aim of this article is to share the management experience of this complex condition with the medical community and to conduct an up-to-date literature review on nodular pulmonary amyloidosis.

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“…Lung mucosa-associated lymphoid tissue (MALT) has been reported, occasionally related to Helicobacter pylori [58,59]. At CT, MALT lymphomas manifest as chronic localized opacities including consolidations, nodules, and masses with the presence of airways within the lesions in 85% [60,61]. After respiratory failure, lymphoma is the second cause of death in CVID [16].…”

Section: Lung Manifestations In Common Variable Immunodeficiencymentioning

confidence: 99%

The Lung in Dysregulated States of Humoral Immunity

Uzunhan¹,

Jeny²,

Kambouchner³

et al. 2017

Respiration

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In common variable immunodeficiency, lung manifestations are related to different mechanisms: recurrent pneumonias due to encapsulated bacteria responsible for diffuse bronchiectasis, diffuse infiltrative pneumonia with various patterns, and lymphomas, mostly B cell extranodal non-Hodgkin type. The diagnosis relies on significant serum Ig deficiency and the exclusion of any primary or secondary cause. Histopathology may be needed. Immunoglobulin (IgG) replacement is crucial to prevent infections and bronchiectasis. IgG4-related respiratory disease, often associated with extrapulmonary localizations, presents with solitary nodules or masses, diffuse interstitial lung diseases, bronchiolitis, lymphadenopathy, and pleural or pericardial involvement. Diagnosis relies on international criteria including serum IgG4 dosage and significantly increased IgG4/IgG plasma cells ratio in pathologically suggestive biopsy. Respiratory amyloidosis presents with tracheobronchial, nodular, and cystic or diffuse interstitial lung infiltration. Usually of AL (amyloid light chain) subtype, it may be localized or systemic, primary or secondary to a lymphoproliferative process. Very rare other diseases due to nonamyloid IgG deposits are described. Among the various lung manifestations of dysregulated states of humoral immunity, this article covers only those associated with the common variable immunodeficiency, IgG4-related disease, amyloidosis, and pulmonary light-chain deposition disease. Autoimmune connective-vascular tissue diseases or lymphoproliferative disorders are addressed in other chapters of this issue.

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Pulmonary mucosa-associated lymphoid tissue lymphoma revisited

Cited by 68 publications

References 96 publications

Endobronchial Mucosa-associated Lymphoid Tissue Lymphoma: A Report of Two Cases and a Review of the Literature

Endobronchial Mucosa-associated Lymphoid Tissue Lymphoma: A Report of Two Cases and a Review of the Literature

Nodular pulmonary amyloidosis: a complex disease with malignancy association

The Lung in Dysregulated States of Humoral Immunity

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