scholarly journals Imaging features of unilateral renal T‐cell lymphoma occurring simultaneously in the urinary bladder wall and contralateral ureter with secondary polycythaemia in a dog

Author(s):  
Marta Soler ◽  
Juan García‐Martinez ◽  
Pablo Barge ◽  
Eliseo Belda ◽  
Amalia Agut

2003 ◽  
Vol 4 (4) ◽  
pp. 252 ◽  
Author(s):  
Jun Ho Choi ◽  
Yong Yeon Jeong ◽  
Sang Soo Shin ◽  
Hyo Soon Lim ◽  
Heoung Keun Kang


1998 ◽  
Vol 22 (3) ◽  
pp. 373-377 ◽  
Author(s):  
Walid A. Mourad ◽  
Salim Khalil ◽  
Amer Radwi ◽  
Amjad Peracha ◽  
Adnan Ezzat




2000 ◽  
Vol 37 (2) ◽  
pp. 184-186 ◽  
Author(s):  
P. Maiolino ◽  
G. DeVico

A 7-year-old, intact female mixed-breed dog was presented for evaluation of hematuria. Physical examination revealed a suprapubic mass. Ultrasonographic examination showed a large lobular mass occupying the urinary bladder. At the owners' request, the dog was euthanatized and a postmortem examination was performed. Necropsy confirmed the presence of a lobular mass of about 5- to 6-cm diameter protruding into the lumen of the bladder. Histologically, the mass was composed of a large number of atypical lymphoid cells in the lamina propria and mucosal epithelium. Immunohistochemically, the neoplastic cells expressed CD3 but not CD79α or keratin and vimentin, supporting a diagnosis of T-cell lymphoma.



2021 ◽  
Vol 11 ◽  
Author(s):  
Suli Yu ◽  
Jianqiang Xu

Primary bone lymphoma (PBL) is a less frequent type of extranodal lymphoma, which is defined as a single skeletal tumor or multiple bone lesions without visceral or lymph node involvement. Most published cases have reported diffused large B cell lymphoma (DLBCL) of PBL, and the prognosis is good after conventional treatment. Primary T-cell lymphoma is extremely rare in the literature. The clinical symptoms, imaging findings, diagnosis, treatment and prognosis of primary T-cell lymphoma of bone are still unclear. The case details a young male patient who was treated for bone tuberculosis and was diagnosed with T-cell lymphoma during an open surgical biopsy. Further imaging evidence showed the lymphoma was localized within the femur. The patient responded poorly to combined chemo- and radiotherapy. He was confirmed with local lung metastases 11 months later and died at the 17th month of onset. I would like to provide PBL entities with some rare information about primary bone peripheral T-cell lymphoma and discuss the best strategy for the treatment of rare PBL subtypes.



2021 ◽  
Author(s):  
Xiaoying Zhang ◽  
Qian Yu ◽  
Ying Liu ◽  
Simin Liu ◽  
Zhongwei Lv

Abstract Background: Monomorphic epitheliotropic intestinal T-cell lymphoma (MEITL) is an uncommon, rapidly progressive, primary intestinal T-cell lymphoma. The most common site of occurrence is the small intestine. The prognosis of MEITL is extremely poor due to late diagnosis and lack of targeted therapy.Case presentation: A case of MEITL involving the entire small bowel, part of colon, rectum, mesenteric lymph nodes and liver is herein reported. We are presenting the 18F-FDG PET/CT features of MEITL, which showed all involved lesions with increased FDG activity. The MRI and pathological characteristics of MEITL were also described. Furthermore, some malignant diseases should be considered in the differential diagnosis. Conclusions: Based on the lesions with high accumulation of FDG, our case shows the involved extent of MEITL, which is helpful for biopsy and treatment option decisions. We expect more and more physicians could know this disease and make an early diagnosis to improve the outcomes of MEITL.



2008 ◽  
Vol 39 (6) ◽  
pp. 15
Author(s):  
BRUCE JANCIN


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