scholarly journals Pleural Nodules and Mediastinal Lymphadenopathy in a Smoker: An Unusual Case Report

2016 ◽  
Vol 9 (2) ◽  
pp. 488-492 ◽  
Author(s):  
Damien Desbuquoit ◽  
Stijn  Van Hecke ◽  
Pjotr Even ◽  
Paul M. Parizel ◽  
Jan P. van Meerbeeck ◽  
...  

The authors report a case of thoracic splenosis, which is the autotransplantation of splenic tissue into the pleural cavity. Splenosis in the chest is a rare entity and most often an incidental finding on chest computed tomography, typically showing solitary or multiple well-defined, noncalcified pleural nodules of variable size in the left hemithorax. It is important to include this benign pathology in the differential diagnosis among other, generally malignant, pleural lesions. Imaging clues to the diagnosis are absence of the spleen and/or associated rib fractures. Early identification of thoracic splenosis as a cause of pleural nodules can prevent unnecessary and risky invasive procedures, such as biopsy or surgery.

2018 ◽  
Vol 7 (5) ◽  
pp. 205846011877232 ◽  
Author(s):  
Doriana Vergara ◽  
Francesco Ginolfi ◽  
Stefano Moscati ◽  
Beniamino Giordano ◽  
Nicola Ferrara ◽  
...  

Hepatic splenosis represents the heterotopic implantation of splenic tissue caused by the spillage of cells from the spleen usually after splenectomy or splenic trauma. This condition is usually an incidental finding during surgery and its real incidence is unknown. Splenic implants, which can be placed anywhere in the abdominal cavity, are usually multiple and may be confused with different benign and malignant conditions such as renal tumors, abdominal lymphomas, and endometriosis. We hereby report an unusual case of multiple abdominal splenosis, with a particular intra-hepatic location, that could be misinterpreted as an hepato-cellular carcinoma.


Author(s):  
Harsha Vardhan Gowthamnath ◽  
J.S. Jesija ◽  
K. Saraswathi Gopal

2016 ◽  
Vol 3 (1) ◽  
pp. 1-4
Author(s):  
Leena James ◽  
Tejavathi Nagaraj ◽  
Haritma Nigam ◽  
Yogesh

2019 ◽  
Vol 02 (03) ◽  
Author(s):  
Tika Ram Bhandari ◽  
Sudha Shahi ◽  
Sarfaraz Alam Khan

2013 ◽  
Vol 2013 ◽  
pp. 1-6 ◽  
Author(s):  
V. Nagalaxmi ◽  
Mithare Sangmesh ◽  
Kotya Naik Maloth ◽  
Srikanth Kodangal ◽  
Vani Chappidi ◽  
...  

Ameloblastoma is a benign odontogenic neoplasm which frequently affects the mandible. The term ameloblastoma includes several clinicoradiological and histological types. Apart from the most commonly encountered clinicopathologic models, there are few variants, whose biological profile is unknown or not elicited. Among these types, unicystic ameloblastoma is the least encountered variant of the ameloblastoma. Unicystic ameloblastoma refers to those cystic lesions that show clinical, radiographic, or gross features of a jaw cyst but on histologic examination show a typical ameloblastomatous epithelium lining the cyst cavity, with or without luminal and/or mural tumor proliferation. Unicystic ameloblastoma is a less encountered variant of the ameloblastoma and is believed to be less aggressive. As this tumor shows considerable similarities with dentigerous cysts, both clinically and radiographically, the biologic behaviour of this tumor group was reviewed. Moreover, recurrence of unicystic ameloblastoma may be long delayed, and a long-term postoperative followup is essential for proper management of these patients. Here we are presenting a case of unicystic ameloblastoma in an 18-year-old female patient.


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