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Generation and Expansion of Primary, Malignant Pleural Mesothelioma Tumor Lines
Published on: April 21, 2022
[Clinical and pathological profile of the pleural malignant mesothelioma: A retrospective study about 30 cases]
M Mlika1, O Lamzirbi1, M Limam2
1Service de Pathologie, Hôpital Abderrahman Mami, 2037 Ariana, Tunisie; Unité de recherche, 12SP18, Ariana, Tunisie.
Background:
The malignant pleural mesothelioma (MPM) is a rare tumour usually associated to asbestos exposure. The delay between the exposure and the occurrence of the cancer can reach 40 years. This caused the pick of incidence described in many countries including Tunisia. The diagnosis is suspected based on clinical features but positive diagnosis is microscopic. Our aim was to describe the clinical and microscopic features of MPM through a single institution experience.
Patients And Methods:
We conducted a retrospective study about 30 MPM diagnosed over a 20-year-period (1995-2015). We included only patients with complete records including clinical, radiologic and microscopic features. All the microscopic diagnoses were reviewed by 2 pathologists. A mean of 12 slides per case was reviewed. The diagnosis was based on the 2015 WHO classification.
Results:
The mean age of the patients was 61 years, average 22 to 80 years. The sex ratio was 6,5. An asbetose exposition was reported in 21 cases. The most frequent symptoms was chest pain reported in 25 cases. Physical exam was normal in 9 cases. It revealed pleural syndorm in most patients (60 %). Imaging findings consisted mainly in diffuse pleural thickening in 17 cases. Twelve tumours were classified as stage I, 3 stage II, 14 stage III et 1 stage IV. Pleural biopsy was performed using needle in 18 cases, through thoracoscopy in 16 cases, thoracotomy in 3 cases and allowed the diagnosis in respectively 7 cases/18, 16 cases/16 and 3 cases/3. A lymph node biopsy was performed through mediastinoscopy in one case and yelded the diagnosis. The diagnosis was performed on surgical specimen in 2 patients: one bullectomy and one right upper lobectomy. The microscopic exam concluded to an EM in 17 cases, sarcomatoid mesothelioma (SM) in 4 cases and biphasic mesothelioma (BM) in 9 cases. Pan-cytokeratin antibody was used in all cases in association with 2 antibodies with positive diagnostic value and 2 antibodies with negative diagnostic value. It was repeated in 15 cases and the most used antibodies were the anti-calretinin and the TTF1. This was due to the lack of fixation in one case and in order to reach a quality criteria in the other cases. Surgical resection was possible in 2 patients. 15 patients were lost of view after a mean follow-up period of 3 months. Thirteen patients died before or during the follow-up.
Conclusion:
This work was about a Tunisian experience in the diagnosis and management of MPM. The major limits faced were the incomplete databases, the small number of patients included. Microsocpic positive diagnosis necessitates a degree of expertise and every laboratory has to determine the most valuable antibodies through its experience in order to optimize the diagnosis and to reduce the delay of diagnosis.
Insights
Malignant pleural mesothelioma (MPM) diagnosis relies on microscopic examination, often delayed by asbestos exposure. This study details clinical and microscopic features of MPM in Tunisia, highlighting diagnostic challenges and the need for experienced pathology services.
Area of Science:
- Oncology
- Pathology
- Public Health
Background:
- Malignant pleural mesothelioma (MPM) is a rare cancer strongly linked to asbestos exposure, with a long latency period.
- MPM incidence is increasing globally, including in Tunisia, necessitating improved diagnostic strategies.
- Diagnosis is primarily based on microscopic examination of pleural tissue.
Purpose of the Study:
- To describe the clinical and microscopic characteristics of malignant pleural mesothelioma (MPM).
- To evaluate the diagnostic process and challenges within a single institution in Tunisia.
- To analyze the utility of various diagnostic methods, including histopathology and immunohistochemistry.
Main Methods:
- A retrospective study of 30 malignant pleural mesothelioma (MPM) cases diagnosed between 1995 and 2015.
- Inclusion of patients with complete clinical, radiological, and pathological data.
- Review of all microscopic diagnoses by two pathologists using the 2015 WHO classification and immunohistochemistry.
Main Results:
- The average patient age was 61 years, with a male predominance (sex ratio 6.5).
- Asbestos exposure was reported in 21 cases; chest pain was the most frequent symptom (25 cases).
- Microscopic examination revealed epithelioid mesothelioma (EM) in 17 cases, sarcomatoid mesothelioma (SM) in 4, and biphasic mesothelioma (BM) in 9, with immunohistochemistry aiding diagnosis.
Conclusions:
- This Tunisian experience underscores the diagnostic challenges of malignant pleural mesothelioma (MPM), including incomplete data and small sample size.
- Accurate microscopic diagnosis requires specialized expertise and careful selection of immunohistochemical markers.
- Optimizing diagnostic protocols and antibody panels is crucial to reduce diagnostic delays for MPM.
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