Left Lumbar Region

2020 ◽  
Author(s):  
Keyword(s):  
Lumbar Region ◽  
Left Lumbar Region

scholarly journals Approach and management of a giant lipoma in the left lumbar region

2015 ◽  
Vol 14 ◽  
pp. 189-193 ◽  
Author(s):  
Giuseppe Andrea Ferraro ◽  
Rosa Salzillo ◽  
Francesco De Francesco ◽  
Francesco D’Andrea ◽  
Gianfranco Nicoletti
Keyword(s):  
Lumbar Region ◽  
Giant Lipoma ◽  
Left Lumbar Region

CSF fistula through the left lumbar region in adult following a ventriculoperitoneal shunt surgery: a rare case report

2010 ◽  
Vol 31 (6) ◽  
pp. 817-820
Author(s):  
Shi-yin Xiao ◽  
Lu Ma ◽  
Bal Krishna Shrestha ◽  
Yue-kang Zhang ◽  
Bo-Yong Mao
Keyword(s):  
Case Report ◽  
Ventriculoperitoneal Shunt ◽  
Rare Case ◽  
Lumbar Region ◽  
Shunt Surgery ◽  
Csf Fistula ◽  
Rare Case Report ◽  
Left Lumbar Region

scholarly journals Retroperitoneal liposarcoma of the intestine: a rare cause of acute abdomen

2021 ◽  
Vol 8 (5) ◽  
pp. 1614
Author(s):  
Vikash C. Tiwari ◽  
Vaibhav Mudhale ◽  
Kulkarni S. Sharang ◽  
Jineshwar Nyamagoud ◽  
Malluru Srividya
Keyword(s):  
Sudden Onset ◽  
Wide Resection ◽  
Lumbar Region ◽  
Retroperitoneal Mass ◽  
Significant Past Medical History ◽  
Current Case ◽  
Retroperitoneal Liposarcoma ◽  
Malignant Mesenchymal Tumor ◽  
Well Differentiated ◽  
Left Lumbar Region

Retroperitoneal liposarcoma is a rare malignant mesenchymal tumor with an incidence of 2.5 per million individuals. It is usually asymptomatic until its large enough to compress the surrounding organs, so its early diagnosis is difficult. In current case a 41 year old male patient with no significant past medical history presented to emergency department with sudden onset of abdominal pain in the left lumbar region. On examination, the abdomen was distended, guarding and rigidity present with tenderness to palpation in the left lumbar region, and no mass was palpated. Abdominal USG revealed a large heterogeneous mass in the left lumbar region. As the origin of the mass was uncertain, the patient was evaluated with CECT of the abdomen which revealed a retroperitoneal mass highly s/o liposarcoma. Given the suspicion of a liposarcoma, the patient underwent an abdominal exploration and there was a retroperitoneal mass of 12x8 cm adherent to the left colon. Wide resection of this mass was done along with left colectomy and the specimen was sent for examination. The histopathology study determined lipomatous tumor well differentiated retroperitoneal liposarcoma. Retroperitoneal liposarcoma is a malignant tumor whose treatment is fundamentally surgical. These tumors tend to be resistant to radiotherapy and/or chemotherapy. Among the most important prognostic factors related to survival is surgery with non-affected margins.

scholarly journals Primitive neuroectodermal tumor of the kidney: a rare case

2021 ◽  
Vol 27 (1) ◽  
Author(s):  
R. Pandey ◽  
R. Batra ◽  
P. Dhaigude ◽  
D. Gupta
Keyword(s):  
Primitive Neuroectodermal Tumor ◽  
Multimodal Therapy ◽  
Left Kidney ◽  
Neuroectodermal Tumor ◽  
Adolescent And Young Adult ◽  
Lumbar Region ◽  
Transperitoneal Approach ◽  
Case Presentation ◽  
Renal Pnet ◽  
Left Lumbar Region

Abstract Background Primitive neuroectodermal tumor commonly occurs in bones and is equivalent to Ewing’s sarcoma. Very few cases have been reported in the literature and they had a very different presentation and very aggressive behavior. Case presentation We present a case of a young 23-year-old male who presented with complaints of pain in left lumbar region of abdomen since 8 months and hematuria off and on. CT scan of the abdomen was done which revealed a large heterogeneously enhancing mass lesion in the left lumbar region arising from the superior and mid-pole of left kidney showing multiple non-enhancing necrotic areas. A diagnosis of left renal cell carcinoma was kept. Through the transperitoneal approach, the left kidney was approached and a left radical nephrectomy was done. The histopathology report revealed the tumor cells to be positive for CD99 and focally positive for Vimentin and negative for cytokeratin thereby making a diagnosis of primary neuroectodermal tumor (PNET). Conclusions Renal PNET is a rare renal malignancy that should be kept in the differential diagnosis of a renal SOL especially when it is a presenting feature in adolescent and young adult. It has a very aggressive course and multimodal therapy has to be considered in its treatment

Meetings of medical societies. Surgical Society and Society of Radiologists of the ATSSR. Joint meeting 15/XI.1936

1937 ◽  
Vol 33 (4) ◽  
pp. 518-522
Author(s):  
N. Sokolov ◽  
V. Osipovsky
Keyword(s):  
Left Kidney ◽  
Joint Meeting ◽  
Lumbar Region ◽  
Lower Pole ◽  
Medical Societies ◽  
Left Lumbar Region

Demonstrated b-th T-v, 23 y., Delivered to 1 chir. cl. GIDUV with severe profuse hematuria. Hematuria was preceded by an injury to the left lumbar region. Hematuria lasted 7 days. The diagnosis of neoplasm of the kidney was made on the basis of anamnesis and palpation of the dense, tuberous lower pole of the left kidney, the absence of indigo on this side, and a pyelogram, which showed a deformed pelvis with blurred contours.

Skin discoloration in acute necrosis of the pancreas

1935 ◽  
Vol 31 (8-9) ◽  
pp. 1118-1118
Author(s):  
I. Н. Zaajеr
Keyword(s):  
Clinical Picture ◽  
Pancreatic Necrosis ◽  
Lumbar Region ◽  
Skin Discoloration ◽  
Left Lumbar Region

The author describes a case of acute pancreatic necrosis, in whose clinical picture the appearance of sharp blue-green spots first in the left lumbar region and then in the circumference of the navel and spreading further was noticed.

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