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Isolation of Human Lymphatic Endothelial Cells by Multi-parameter Fluorescence-activated Cell Sorting
Published on: May 1, 2015
Lymphoid Interstitial Pneumonia and Other Benign Lymphoid Disorders
Antonella Arcadu1, Teng Moua2, Eunhee S Yi3
1Department of Respiratory Disease, University of Sassari, Sassari, Italy.
Benign pulmonary lymphoid disorders are rare conditions with overlapping features. This review details their histopathology, epidemiology, and clinical presentation to aid diagnosis and management.
Area of Science:
- Pulmonology
- Pathology
- Oncology
Background:
- Benign pulmonary lymphoid disorders encompass rare conditions with polyclonal lymphoid infiltrates.
- These disorders present diverse histopathologic, clinicoradiologic, and epidemiologic features that can overlap.
- Accurate diagnosis is challenging and relies heavily on histological examination to differentiate from other conditions.
Purpose of the Study:
- To review the histopathological, epidemiological, and clinicoradiologic characteristics of various benign pulmonary lymphoid disorders.
- To provide a comprehensive overview to aid in the diagnosis and management of these rare lung conditions.
Main Methods:
- Literature review and synthesis of existing data on benign pulmonary lymphoid disorders.
- Focus on histopathological patterns, epidemiological trends, and clinical/radiological manifestations.
Main Results:
- Detailed descriptions of specific disorders including lymphoid interstitial pneumonia, follicular bronchiolitis, nodular lymphoid hyperplasia (pulmonary pseudolymphoma), inflammatory pseudotumor, immunoglobulin G4-related disease, Castleman disease, posttransplantation lymphoproliferative disease, and drug-induced lymphoid disorders.
- Emphasis on the diagnostic challenges posed by overlapping features and the critical role of histopathology.
Conclusions:
- Histological examination is crucial for diagnosing benign pulmonary lymphoid disorders and excluding other causes.
- Further research into pathogenesis and clinical trials are necessary to guide therapeutic strategies for these rare conditions.
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