A Rare Presentation of a Rare Disease: Pulmonary Lymphomatoid Granulomatosis
Author(s) -
Ghulam Rehman Mohyuddin,
Fatima Sultan,
Ghulam Khaleeq
Publication year - 2012
Publication title -
case reports in pulmonology
Language(s) - English
Resource type - Journals
eISSN - 2090-6846
pISSN - 2090-6854
DOI - 10.1155/2012/371490
Subject(s) - medicine , lymphomatoid granulomatosis , chest radiograph , rare disease , presentation (obstetrics) , bronchus , radiology , lung , biopsy , sarcoidosis , radiography , right main bronchus , pathology , disease , respiratory disease
A 70-year-old female presented with a 4-week history of dry cough and wheezing. Chest radiograph showed a 10.5 cm mass-like density in the anterior mediastinum which had not been previously visualized. Computed tomography scan (CT) of the chest showed a right hilar mass encasing and narrowing right upper lobe bronchus and right mainstem bronchus and secondary atelectatic changes. Biopsy was consistent with a diagnosis of lymphomatoid granulomatosis Grade 3. She responded well clinically and radiologically to therapy. Lymphomatoid granulomatosis is a rare EBV-associated disorder which is considered a lymphoproliferative disease. The most common radiographic feature is multiple lung nodules. An isolated hilar mass is an exceptionally rare presentation of this rare disease.
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