Non-Hodgkins lymphoma in a patient with tracheal bronchus who presented with atypical pneumonia: a diagnostic dilemma
- 1Department of Cardiothoracic Surgery, Northwestern Deanery, Manchester, UK
- 2Department of Respiratory Diseases, Blackpool Victoria Hospital, Blackpool, UK
- 3Department of Neuropathology, Lancashire Teaching Hospitals, Preston, UK
- 4Department of Cardiothoracic Surgery, Blackpool Victoria Hospital, Blackpool, UK
- Correspondence to Mr Nnamdi Nwaejike,
A 47-year-old unemployed man presented with a 2-week history of shortness of breath, dry cough and fever despite normal inflammatory markers and negative blood cultures. There was no weight loss or night sweats. He was a non-smoker and had no other medical history. HIV testing and tumour markers were negative.
Chest x-ray (figure 1A) showed what seemed to be a dense consolidation in the right mid-zone and lower zone. This was confirmed on CT (figure 1F), so wedge biopsies of the right middle and right lower lobes were taken via video-assisted thoracoscopy (VATS). There were no palpable lymph nodes and no evidence of significant mediastinal lyphadenopathy on CT (figure 1C–E). Bronchoscopy at the time of VATS showed a tracheal (pig) bronchus with the right upper lobe bronchus arising separately from the trachea (figure 1B).
Postoperative course was uneventful and he was discharged in good health to the respiratory physicians on day 3. There was no definitive diagnosis following histopathological examination of the lung biopsies. Cultures of the biopsies were negative for any pathogens. With no definite diagnosis, he received nebulisers and oxygen in the interim but subsequently developed seizures requiring intubation and ventilation. MRI, at this time, showed lesions in the brain and he continued to deteriorate and eventually passed away.
Postmortem examination showed high-grade non-Hodgkins lymphoma—B-cell type predominantly affecting the brain but also infiltrating the lungs, heart, liver, kidneys and urinary bladder (figure 2).
In patients with known non-Hodgkins lymphoma (NHL) and pulmonary infiltrates, lung biopsy yields specific diagnoses in only 50% of cases.1 Secondary involvement of the lung in patients with lymphoma has an incidence of 25–40%.2 A disappointing reminder of the limitations of lung biopsy as an aid to definite diagnosis for pathology involving the lung parenchyma.
This patient had symptoms and signs of interstitial lung disease. There were no palpable lymph nodes and no significant mediastinal lyphadenopathy on CT to indicate lymph node biopsy for diagnosis by mediastinoscopy. Unfortunately, this patient had no other symptoms or signs to suggest pathology elsewhere, until seizures led to an MRI showing lesions in the brain. Tumour markers remained negative.
An atypical presentation of fevers and mass effect (pneumonitis in this case) without other typical symptoms of fatigue, weight loss or night sweats should elicit a high degree of suspicion for lymphoma and appropriate whole body scanning initiated to aid in diagnosis. Even with inconclusive results from lung biopsy, other sources of tissue diagnosis must be sought. Delays in definitive diagnosis can lead to an unfortunate outcome.3