Atypical Appearance of Pneumocystis carinii pneumonia Without Ground-Glass Opacities
Article Information
Aatif Amir Husain1*, Rahul Khamar2, Raees Lunat3, Ruhaid Khurram4
1Intensive Care Department, Imperial College Healthcare NHS Trust, United Kingdom
2Radiology Department, Guy's and St Thomas' NHS Foundation Trust, United Kingdom
3Accident and Emergency Department, Royal Free London NHS Foundation Trust, United Kingdom
4Radiology Department, Royal Free London NHS Foundation Trust, United Kingdom
*Corresponding Author: Dr. Aatif Amir Husain, Intensive Care Department, Imperial College Healthcare NHS Trust, United Kingdom
Received: 24 September 2020; Accepted: 07 October 2020; Published: 10 October 2020
Citation: Aatif Amir Husain, Rahul Khamar, Raees Lunat, Ruhaid Khurram. Atypical Appearance of Pneumocystis carinii pneumonia Without Ground-Glass Opacities. Journal of Radiology and Clinical Imaging 3 (2020): 089-091.
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Keywords
Pneumocystis; Computed Tomography; Ground-glass; HIV; Atypical Pneumonia
Article Details
Main Point
This article serves to demonstrate Pneumocystis carinii pneumonia may cause severe infection and significant lung changes on computerized tomography scan without containing its hallmark feature - ground-glass opacities.
Clinical Image
A 51-year-old male with a background of advanced HIV and non-compliance with antiretrovirals was referred to the infection team with a 4-month history of cough, dyspnoea, 2-stone weight loss and night sweats. On admission, his viral load was greater than 1 million copies with a CD4+ T cell count of 0.056 ´ 109/L (normal range 0.3 - 1.4 x109/L). Notably, his Beta D Glucan serology and Lactate Dehydrogenase levels were 455.6 pg/mL (<80 pg/mL) and 189 unit/mL (135 – 225 unit/mL), respectively. A contrast-enhanced examination of the chest (Figure 1) revealed widespread nodularity measuring up to 12mm in diameter with areas of cavitation measuring up to 30mm. There was no zonal predominance. An infectious aetiology was strongly suspected however appearances were not in-keeping with key differentials. There was no ground-glass opacification to suggest pneumocystis or cytomegalovirus pneumonia; no significant lymphadenopathy or central cavity calcification to suggest histoplasmosis and no necrotic lymph nodes to implicate TB. Furthermore, the lack of bronchiectatic change and diffuse nature of the nodularity were not in-keeping with mycobacterium avium complex. Following the result of a bronchoalveolar lavage which was PCR positive for pneumocystis carinii, the patient was initiated on a treatment course of co-trimoxazole. Repeat cross-sectional imaging performed 82-days following the initial scan (Figure 2) revealed significant interval resolution of the nodular and cavitating lesions. This case highlights the importance of considering a wide differential when evaluating aetiologies of lung nodularity and cavitation; specifically, the possibility of pneumocystis presenting without its hallmark ground-glass opacification.