Giant retroperitoneal hemolymphangioma: A case report and review of literature.

World J Clin Cases

Department of Urology, The First Hospital of Shanxi Medical University, Taiyuan 030001, Shanxi Province, China.

Published: August 2024

Background: Hemolymphangioma is a very rare benign tumor in clinical practice caused by abnormalities of the vasculature. Its clinical features are often atypical, and it is easy to miss and misdiagnose. When the time of nuclear magnetic T1 is significantly reduced, the diagnosis of hemangioma should be considered. Therefore, we report this case in the hope of raising clinicians' awareness of the disease.

Case Summary: A 37-year-old man presented with a giant retroperitoneal hemolymphangioma. Computed tomography and magnetic resonance imaging indicated the possibility of a large perirenal lymphatic cyst. The postoperative pathological diagnosis is retroperitoneal hemolymphangioma. The patient underwent surgical excision after adequate drainage. The postoperative recovery was smooth and there were no complications. There was no recurrence during half a year of follow-up.

Conclusion: This case reiterates that large retroperitoneal cystic masses with significantly shortened nuclear T1 time should be considered hemolymphangioma. Specific clinical basis and experience for the diagnosis and treatment of these diseases is necessary.

Download full-text PDF

Source
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC11238797PMC
http://dx.doi.org/10.12998/wjcc.v12.i22.5258DOI Listing

Publication Analysis

Top Keywords

retroperitoneal hemolymphangioma
12
giant retroperitoneal
8
hemolymphangioma
5
hemolymphangioma case
4
case report
4
report review
4
review literature
4
literature background
4
background hemolymphangioma
4
hemolymphangioma rare
4

Similar Publications

Background: Hemolymphangioma is a very rare benign tumor in clinical practice caused by abnormalities of the vasculature. Its clinical features are often atypical, and it is easy to miss and misdiagnose. When the time of nuclear magnetic T1 is significantly reduced, the diagnosis of hemangioma should be considered.

View Article and Find Full Text PDF

Rationale: Hemolymphangioma of the pancreas is an extremely rare benign tumor; only 10 patients with this disease have been reported to date, the majority of whom were women.

Patient Concerns: We describe a 28-year-old man who presented with abdominal pain and discomfort. Computed tomography and magnetic resonance imaging data showed a huge heterogeneous solid cystic mass at the retroperitoneal pancreatic head.

View Article and Find Full Text PDF

Introduction: Hemolymphangioma, a rare vascular developmental condition, is characterized by malformed venous and lymphatic components in various proportions. Herein, we report a case of a retroperitoneal cystic tumor in an adult patient.

Presentation Of Case: A 68-year-old man presented to our hospital with complaints of abdominal pain and vomiting.

View Article and Find Full Text PDF

Multiple Hemolymphangioma of the Visceral Organs: A Case Report and Review of the Literature.

Medicine (Baltimore)

July 2015

From the Department of Hepatobiliary Surgery, First Affiliated Hospital of Bengbu Medical College (D-YZ, ZL, XM, W-LS,WW, P-YC); Department of Bengbu Medical College, Bengbu, Anhui, China (Q-YW).

Hemolymphangioma is a rare disease with malformation of both lymphatic and vascular vessels. Few cases of hemolymphangioma occurring in the rectum, small intestine, pancreas, esophagus, and other organs have been reported. Nevertheless, multiple hemolymphangioma of the visceral organs are extremely rare.

View Article and Find Full Text PDF

Want AI Summaries of new PubMed Abstracts delivered to your In-box?

Enter search terms and have AI summaries delivered each week - change queries or unsubscribe any time!