Squamous Cell Lung Cancer Complicating a Tuberculous Fibrothorax





History of Present Illness


An 82-year-old man presented to the outpatient pulmonary clinic because in the past 4 weeks he had worsening breathlessness and low-grade fever. He also had a mild, chronic, cough without sputum and had a weight loss of about 3 kg in 3 months. Chest radiography, ordered by his general practitioner, revealed bilateral calcified pleural plaques, more on the right than on the left, and further opacity in the right mid-zone ( Fig. 4.1 ).




Fig. 4.1


Posteroanterior chest radiograph showing bilateral pleural thickening, with calcific plaques caused by fibrothorax. Additional opacity in the right mid-zone and volume loss of the right thorax, with mild mediastinal shift to the right, are also evident.


Past Medical History


The patient had never smoked and had worked as a truck driver. When he was 25 years old, he had been diagnosed with pulmonary tuberculosis and had undergone artificial right pneumothorax. His medical history also included arterial hypertension and prostatic hypertrophy.


Physical Examination and Early Clinical Findings


The patient was hemodynamically stable, with oxygen saturation of 93% in room air and body temperature of 37.2° C [98.9° F]. Physical examination revealed widely reduced breath sounds, mainly on the right side, and fine crackles at the lower zones. Recent blood tests had shown slight leukocytosis (white blood cell [WBC] count: 12,500 cells/μL, with 59.6% neutrophils and 31.8% lymphocytes) and a small increase in the inflammation indices (C-reactive protein [CRP]: 28 mg/L, normal values < 5 mg/L). No results of previous chest computed tomography (CT) or x-ray were available. Chest ultrasonography ( Fig. 4.2 ) showed narrowed intercostal spaces, whereas the pleural line and the gliding sign were difficult to observe. At the right base, an anechoic area compatible with fluid collection was appreciated.




Fig. 4.2


Chest ultrasound showing layers of the thorax and the interface between the lung and the pleura, which are difficult to distinguish because of fibrothorax. A hypogenic area compatible with fluid collection is also noticeable.


Chest CT showed a round mass with smooth margins and a nonhomogeneous fluid content, located in the posterior region of the right lower lobe, contiguous with the calcified fibrothorax ( Figs. 4.3 , A–C ).




Fig. 4.3


Chest computed tomography (CT) scan (soft tissue window) in the axial (A), coronal (B), and sagittal (C) planes. Diffuse, sheet-like pleural calcification, caused by calcified fibrothorax, and volume loss of the right lung are evident. A round mass with smooth margins and nonhomogeneous fluid content is present in the posterior region of the right lower lobe.


The patient was admitted for further investigations. Thoracic ultrasonography allowed for identification of a space among the pleural calcifications, through which a 14-gauge needle was introduced until it reached the fluid collection. Passage of the needle through the thickened and calcified pleura was difficult. Only 5 mL of odorless, beige-colored liquid was extracted. In this sample, microscopic examination for acid-fast bacilli (AFB) yielded negative results, as did polymerase chain reaction (PCR) amplification of relevant DNA sequences of Mycobacterium tuberculosis. Sputum and urine smear microscopy results were also negative for AFB.


Whole-body 18 fluorodeoxyglucose (FDG) positron emission tomography (PET) was performed ( Fig. 4.4 ). The lesion in the right lower lobe showed intense uptake in its peripheral part, with a maximum standard uptake value (SUV max ) of 6. No abnormal accumulation of the 18 FDG was found in other parts of the body.


Jun 19, 2021 | Posted by in RESPIRATORY | Comments Off on Squamous Cell Lung Cancer Complicating a Tuberculous Fibrothorax

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