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Detection of Invasive Pulmonary Aspergillosis in Haematological Malignancy Patients by using Lateral-flow Technology
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[Pulmonary malt lymphoma].

Raphaël Borie1, Martine Antoine2, Jacques Cadranel3

  • 1Service de pneumologie A, centre de compétences maladies rares pulmonaires, AP-HP hôpital Bichat-Claude Bernard, 46, rue Henri Huchard, 75877 Paris cedex 18, France.

Bulletin Du Cancer
|February 11, 2014
PubMed
Summary
This summary is machine-generated.

Pulmonary MALT lymphoma, a common low-grade B cell lymphoma of the lung, arises from mucosa-associated lymphoid tissue. Diagnosis and treatment vary, with a generally good prognosis for this lung cancer.

Keywords:
chronic alveolar opacityclonalityoncogenetranslocation

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Area of Science:

  • Oncology
  • Hematology
  • Pulmonology

Context:

  • Pulmonary MALT lymphoma is the most frequent type of lymphoma originating in the lung.
  • It is a low-grade B cell lymphoma derived from mucosa-associated lymphoid tissue.
  • Unlike other MALT lymphomas, no specific pathogen is linked to the pulmonary form.

Purpose:

  • To review current knowledge on the pathophysiology, diagnosis, prognosis, and treatment of pulmonary MALT lymphoma.
  • To highlight key diagnostic methods, including minimally invasive procedures.
  • To discuss the range of treatment options available.

Summary:

  • Pulmonary MALT lymphoma presents asymptomatically with chronic alveolar opacities.
  • Diagnosis relies on histology obtained via bronchoscopy or CT-guided biopsy.
  • Translocations involving the MALT1 gene are common, though no pathogen association exists.

Impact:

  • Provides a comprehensive overview for clinicians managing pulmonary MALT lymphoma.
  • Aids in understanding the diagnostic challenges and therapeutic strategies.
  • Contributes to improved patient outcomes through informed management decisions.