Papillary Mesothelioma of Pleura: Case Report
Journal Title: Scholars Journal of Medical Case Reports - Year 2014, Vol 2, Issue 8
Abstract
Papillary mesothelioma of pleura is a rarely observed well-differentiated subtype of epithelial mesothelioma which is a less aggressive, slow growing cancer that does not typically metastasize (spread) to other parts of the body. We report a 55 year old male, farmer by occupation, presented with complaints of breathlessness, cough with expectoration, left-sided chest pain and generalized weakness for 3 months with no history of asbestos exposure nor any lung disease in family. On systemic examination there was restricted chest wall movement on left side with left side bulging of chest, there was decreased breath sounds and presence of stony dullness. Chest X-ray and CT chest revealed left-sided massive pleural effusion. Thoracoscopy guided pleural biopsy was taken which confirmed the diagnosis of papillary mesothelioma.Papillary mesothelioma is well described in the literature, with most reported cases arising from the peritoneum in women of reproductive age. Although less common, doctors have found papillary mesothelioma growth on several of the body’s protective membranes, including the linings of the lungs (pleura), heart (pericardium) and testicles (tunica vaginalis). Unlike malignant mesotheliomas, which are typically associated with asbestos exposure, there is no conclusive evidence linking papillary mesothelioma to asbestos exposure. We conclude that papillary mesothelioma is a rare and unusual mesothelial tumor, characterized by a no evident linkage with asbestos exposure, lack of deep invasion and associated with an indolent clinical course, better prognosis with absence of metastasis and long survival. Keywords: Malignant pleural mesothelioma (MPM), Pleura, Thoracoscopy, Pleural biopsy
Authors and Affiliations
Sandip Patel, Ashwin Rajbhoj, Kulbhushan Marathe, Tanmai Yermal, Amit Thopte, M. A Ghanekar
Squamous Cell Carcinoma Arising From a Mature Cystic Teratoma of Ovary: A Rare Case
Mature cystic teratoma accounts for 10-20 % of all ovarian tumors. Malignant transformation is very rare in mature cystic teratoma, its incidence being 1-2% and is commonly seen in post menopausal women with tumor size l...
Heart as an Early Site of Metastasis from Squamous Cell Carcinoma of Occult Primary: Rare Case Report
Cardiac involvement by primary and secondary tumors is one of the least investigated subjects in oncology. Metastasis of squamous cell carcinoma (SCC) is rare and so is the bilateral ventricular involvement. We report a...
Omental Torsion: A Rare Cause of Acute Abdomen
Omental torsion is an extremely rare differential diagnosis of acute abdomen. It usually requires surgical intervention. More often it is diagnosed Intraoperative and treatment by resection is current management of choic...
Hydatid Cyst of the Adductor Compartment (About a Case with Literature Review)
The hydatid cyst is a common zoonosis affecting humans and many mammals that are related to the development of the larval form of a dog cestode: Echinococcus Granulosus (EG). Muscle localization of hydatid cysts remains...
Infantile Pompes disease in a female neonate with significant family history: A case report
Abstract: Pompes disease is a rare metabolic myopathy of autosomal recessive inheritance. It is caused by the deficiency of lysosomal enzyme acid alpha-glucosidase, which results in lysosomal and cytoplasmic glycogen acc...