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Clinical Image

Volume 5, Issue 10 (October Issue)

Pulmonary Cavitary Lesions Revealing a Rare Tumor

Hana Blibech1*, Houda Snene1, Yossr Aloulou1, Donia Belkhir1, Nadia Mehiri1, Aida Ayadi2, Adel Marghli3, Nozha Ben Salah1 and Bechir Louzir1

1Pulmonology Department, Mongi Slim Hospital University of Tunis El Manar Faculty of Medicine of Tunis, Tunis, Tunisia
2Pathology Department, Abderrahmen Mami Hospital, Faculty of Medicine of Tunis, University of Tunis El Manar, Tunis, Tunisia
3Thoracic Surgery Department, Abderrahmen Mami Hospital, University of Tunis El Manar Faculty of Medicine of Tunis, Tunis, Tunisia

*Corresponding author: Hana Blibech, Pulmonology Department, Mongi Slim Hospital University of Tunis El Manar Faculty of Medicine of Tunis, Tunis, Tunisia. E-mail:

Received: September 27, 2023; Accepted: October 13, 2023; Published: October 25, 2023

Citation: Blibech H, Snene H, Aloulou Y, et al. Pulmonary Cavitary Lesions Revealing a Rare Tumor. Clin Image Case Rep J. 2023; 5(10): 352.

Pulmonary Cavitary Lesions Revealing a Rare Tumor

A 36-year-old man, previously healthy but with a 20-year smoking history, presented with a persistent six-month cough and blood-streaked sputum. He also experienced intermittent fever and fatigue. A chest X-ray revealed excavated, heterogeneous opacities in the left parahilar region. A chest CT scan further showed cavitary, irregular consolidation in the lingular lung area, with surrounding ground-glass opacities, nodules, and excavated nodules (Figure 1: A+B).

Initial discussed diagnoses included tuberculosis, aspergillosis, granulomatosis with polyangitis, or a lung tumor. Bronchoscopy revealed no abnormalities, and both bacilloscopic and mycological tests on bronchial fluid were negative. Bronchial biopsies showed inflammation, while immunological tests for vasculitis yielded normal results.

Despite not seeking medical attention for six months, the patient's condition did not improve. A follow-up chest CT, conducted six months later, showed persistent consolidation in the lingula, along with increased excavation size and the appearance of new excavated nodules in the lingula and an enlargement of mediastinal adenomegaly (Figure 1: C+D).

Surgical lung biopsy was decided. Exploration revealed extensive mediastinal infiltration and sub-aortic and hilar lymph nodes which were biopsied. Pathological examination confirmed the presence of an undifferentiated tumour proliferation within a lymphoid stroma rich in lymphocytes (Figure 2), specifically lymphoepithelioma-like carcinoma (LELC) with reactive lymph nodes Immunohistochemistry tests indicated positive cytokeratin, negative TTF-1, negative P40, and positive LMP1, supporting the diagnosis of LELC with associated EBV infection.

An immunohistochemical study found 80% PDL1-positive cells. Fluorescence in situ hybridization for ROS1 and ALK rearrangements was negative, and Next-Gen Sequencing showed a KRAS mutation (G13S).

LELC is a non-keratinizing carcinoma commonly found in the nasopharynx and foregut-derived organs like the stomach, thymus, and liver. Literature reports show approximately 56.22% in the nasopharynx, 21.32% elsewhere in the head and neck, and 7.83% in other body areas. Primary pulmonary LELC represents just 0.9% of all lung cancers [1]. It often resembles bronchial carcinoma, presenting as a solid lung tissue mass [2].

Keywords: Lymphoepithelioma-like carcinoma; Lung carcinoma; Cavity; Computed tomography