scholarly journals PRIMARY LEIOMYOSARCOMA OF URINARY BLADDER- A RARE PRESENTATION IN POSTPARTUM PERIOD

2016 ◽  
Vol 3 (101) ◽  
pp. 5596-5599
Author(s):  
Sauda V. M ◽  
Ashida M Krishnan
2000 ◽  
Vol 8 (1) ◽  
pp. 67-69 ◽  
Author(s):  
Madhava Janardhan Naik ◽  
Chong Hee Lim ◽  
Thirugnanam Agasthian

An unusual case of primary leiomyosarcoma presenting as a cystic mass is reported. An 86-year-old man underwent resection of a large cystic mass measuring 15 cm in diameter, arising from the left lower lobe of the lung. Histology of the resected specimen showed primary pulmonary leiomyosarcoma. The patient made a good recovery.


2015 ◽  
Vol 2015 (4) ◽  
pp. rjv045-rjv045
Author(s):  
K. R. Shrestha ◽  
B. R. Luitel ◽  
U. Shrestha ◽  
U. K. Shrestha

Author(s):  
Swati Saini ◽  
Monika Garg ◽  
Shaina Goyal ◽  
Anita Chaudhary

AbstractLymphoepithelioma-like carcinoma of the urinary bladder is a rare variant of urothelial carcinoma that was first described by Zukerberg in 1991 and confirmed as a type of urothelial carcinoma by the WHO classification of the urinary system tumors. A 63-year-old man presented with the chief complaint of gross hematuria for 2 months. Sections from transurethral resection of the bladder revealed urothelial carcinoma. A radical cystoprostatectomy was performed and a final histopathological examination revealed high-grade muscle-invasive urothelial carcinoma, lymphoepithelial variant. The patient has been receiving adjuvant chemotherapy with no recurrence reported to date. This is the third case reported in India to date to the best of our knowledge. Owing to its rare presentation, no definite treatment guidelines have been established for this entity. Various studies from the English literature suggest a conservative approach.


2020 ◽  
Vol 13 (9) ◽  
pp. e235353
Author(s):  
Neethu Sunil V ◽  
Kevin John ◽  
Sultan Nawahirsha ◽  
Ramya Iyyadurai

A 68-year-old woman presented with episodes of headache, palpitations, sweating and poorly controlled hypertension for the past 6 years. These symptoms were, at times, associated with micturition, and there were few episodes of micturition syncope as well. She had elevated 24-hour urinary normetanephrine and was found to have a paraganglioma arising from the urinary bladder infiltrating the sigmoid colon. She underwent laparotomy with excision of the bladder paraganglioma, following which her symptoms subsided. Paragangliomas are extra-adrenal catecholamine-producing tumours. Bladder paragangliomas need to be considered when evaluating hypertensive patients with headache, palpitations or syncope related to micturition.


2014 ◽  
Vol 41 (1) ◽  
pp. 62-63
Author(s):  
M Akteruzzaman ◽  
Z Islam ◽  
S Afroza ◽  
ARML Kabir ◽  
SK Paul ◽  
...  

A 30 months old boy presented with polyuria and polydipsia since 6 months of age. There was no family history of similar illness. Investigations revealed serum hyperosmolarity and normal renal function. Diagnostic findings correlated with nephrogenic diabetis insipidus (NDI) as the patient was non-responsive to vasopressin in water deprivation test. MRI of brain was normal and ultrasonogram of kidney, ureter, and urinary bladder was normal and other investigations showed no abnormality. DOI: http://dx.doi.org/10.3329/bmj.v41i1.18788 Bangladesh Medical Journal 2012 Vol. 41 No. 1; 62-63


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