Lymphocytic interstitial pneumonitis

Case contributed by Hani Makky Al Salam
Diagnosis certain

Presentation

Known case of connective tissue disease. Complaining of gradual onset of progressive dyspnea.

Patient Data

Age: 25
Gender: Female

2012

x-ray

Low lung volume.

Bilateral ground glass nodules and small cysts. Mild interstitial lung changes. 

2013

x-ray

Low lung volume.

2014

x-ray

Low lung volume. 

2015

x-ray

Low lung volume.

Axillary and medistinal lymphadenopathy. Scattered bilateral small thin wall cysts and ground glass nodules. Some of the nodules demonstrates cystic degeneration at the interval. Mild interstitial lung changes. 

Case Discussion

The patient known case of MCTD, SLE, Sjogren syndrome.

This case demonstrates interval degeneration of multiple pre-existing ground glass nodules into emphysematous cysts with millimeter thick walls.  Interval growth of the pre-existing bilateral pulmonary cysts.  Interval development of new bilateral scattered ground glass nodules and interval development of non-specific irregular solid subpleural nodule in the left lower lobe.  Grossly unchanged bilateral axillary and mediatinal lymphadenopathy.  Among the differential diagnostic considerations one should consider Wegener's granulomatosis and lymphocytic interstitial pneumonitis.  If the patient is immunocompromised, PCP and fungal pneumonia should be considered.  Finally, lymphoproliferative disorders and cystic metastases to the lung parenchyma should be excluded.

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