Progression of a rare multiple cystic lung disease

Differential diagnosis of multiple cystic lung disease:[1] LymphangioleiomyomatosisPulmonary Langerhans cell histiocytosis (PLCH)Folliculin gene-associated syndrome: Extrapulmonary symptoms can occur in 10%-15% of these patients with skin rashes, lymphadenopathy, bone pains, or diabetes insipidus (h...

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Published in:Lung India Vol. 34; no. 4; pp. 393 - 394
Main Authors: Gera, Kamal, Lall, Ajay, Kulshrestha, Ritu, Singh, Kanika, Chhabra, Nandini
Format: Journal Article
Language:English
Published: India Medknow Publications & Media Pvt. Ltd 01.07.2017
Medknow Publications & Media Pvt Ltd
Wolters Kluwer Medknow Publications
Subjects:
Cysts
Hospitals
Lung diseases
Patients
Radiology Quiz
Thorax
Tomography
X-rays
ISSN:0970-2113, 0974-598X
Online Access:Get full text
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Summary:Differential diagnosis of multiple cystic lung disease:[1] LymphangioleiomyomatosisPulmonary Langerhans cell histiocytosis (PLCH)Folliculin gene-associated syndrome: Extrapulmonary symptoms can occur in 10%-15% of these patients with skin rashes, lymphadenopathy, bone pains, or diabetes insipidus (hypothalamic involvement). Clinical-radiologic-pathologic correlation of smoking-related diffuse parenchymal lung disease.
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ISSN:0970-2113
0974-598X
DOI:10.4103/lungindia.lungindia_530_16