A Rare Case of Huge Renal Leiomyosarcoma and Imaging Diagnostic Dilemma
Soft tissue sarcomas are rare mesenchymal tumours. Leiomyosarcoma is a rare malignant tumour of smooth muscle origin that generally arises from soft tissues and uterine tissue. On occasions, they may arise from smooth muscle of the vessel walls, more commonly from the veins. Renal leiomyosarcomas fr...
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doaj-7c813d2653564cd4836a0dc807ed6c502020-11-24T23:08:52ZengJCDR Research and Publications Pvt. Ltd.International Journal of Anatomy Radiology and Surgery2277-85432455-68742017-10-0164RC07RC0910.7860/IJARS/2017/28241:2314A Rare Case of Huge Renal Leiomyosarcoma and Imaging Diagnostic DilemmaAmol Madanlal Lahoti0Gurnihal Singh Chawla1Avinash Dhok2Jitesh Rawat3Kishor Nemade4Junior Resident, Department of Radiology, NKP SIMS and LMH, Nagpur, Maharashtra, India.Senior Resident, Department of Radiology, NKP SIMS and LMH, Nagpur, Maharashtra, India.Professor and Head, Department of Radiology, NKP SIMS and LMH, Nagpur, Maharashtra, India.Senior Resident, Department of Radiology, NKP SIMS and LMH, Nagpur, Maharashtra, India.Junior Residen, Department of Radiology, NKP SIMS and LMH, Nagpur, Maharashtra, India.Soft tissue sarcomas are rare mesenchymal tumours. Leiomyosarcoma is a rare malignant tumour of smooth muscle origin that generally arises from soft tissues and uterine tissue. On occasions, they may arise from smooth muscle of the vessel walls, more commonly from the veins. Renal leiomyosarcomas frequently originates from the smooth muscles of renal capsule, renal pelvis or renal vessels. Correct diagnosis and appropriate management is very essential in such cases. We highlight the possibility of malignant soft tissue sarcoma like leiomyosarcoma in the kidney. We emphasize on the suspicion of rare possibility and clinicopathological correlation is required to identify such cases, which has pronounced prognostic implications as whether to do surgical resection or biopsy or treat such patient with chemotherapy or radiotherapy vary with diagnosis.http://www.ijars.net/articles/PDF/2314/28241_CE[VSU]_F(GH)_PF1(VSUAK)_NC_(VSU_GG)_PF2(VSU_GG).pdfMesenchymal tumourNeuroectodermal tumourSarcomas |
collection |
DOAJ |
language |
English |
format |
Article |
sources |
DOAJ |
author |
Amol Madanlal Lahoti Gurnihal Singh Chawla Avinash Dhok Jitesh Rawat Kishor Nemade |
spellingShingle |
Amol Madanlal Lahoti Gurnihal Singh Chawla Avinash Dhok Jitesh Rawat Kishor Nemade A Rare Case of Huge Renal Leiomyosarcoma and Imaging Diagnostic Dilemma International Journal of Anatomy Radiology and Surgery Mesenchymal tumour Neuroectodermal tumour Sarcomas |
author_facet |
Amol Madanlal Lahoti Gurnihal Singh Chawla Avinash Dhok Jitesh Rawat Kishor Nemade |
author_sort |
Amol Madanlal Lahoti |
title |
A Rare Case of Huge Renal Leiomyosarcoma and Imaging Diagnostic Dilemma |
title_short |
A Rare Case of Huge Renal Leiomyosarcoma and Imaging Diagnostic Dilemma |
title_full |
A Rare Case of Huge Renal Leiomyosarcoma and Imaging Diagnostic Dilemma |
title_fullStr |
A Rare Case of Huge Renal Leiomyosarcoma and Imaging Diagnostic Dilemma |
title_full_unstemmed |
A Rare Case of Huge Renal Leiomyosarcoma and Imaging Diagnostic Dilemma |
title_sort |
rare case of huge renal leiomyosarcoma and imaging diagnostic dilemma |
publisher |
JCDR Research and Publications Pvt. Ltd. |
series |
International Journal of Anatomy Radiology and Surgery |
issn |
2277-8543 2455-6874 |
publishDate |
2017-10-01 |
description |
Soft tissue sarcomas are rare mesenchymal tumours. Leiomyosarcoma is a rare malignant tumour of smooth muscle origin that generally arises from soft tissues and uterine tissue. On occasions, they may arise from smooth muscle of the vessel walls, more commonly from the veins. Renal leiomyosarcomas frequently originates from the smooth muscles of renal capsule, renal pelvis or renal vessels. Correct diagnosis and appropriate management is very essential in such cases. We highlight the possibility of malignant soft tissue sarcoma like leiomyosarcoma in the kidney. We emphasize on the suspicion of rare possibility and clinicopathological correlation is required to identify such cases, which has pronounced prognostic implications as whether to do surgical resection or biopsy or treat such patient with chemotherapy or radiotherapy vary with diagnosis. |
topic |
Mesenchymal tumour Neuroectodermal tumour Sarcomas |
url |
http://www.ijars.net/articles/PDF/2314/28241_CE[VSU]_F(GH)_PF1(VSUAK)_NC_(VSU_GG)_PF2(VSU_GG).pdf |
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