Evidence map›Paper›PMID 39109033›Full record

ArticleWorld journal of clinical cases2024

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

Yi-Kai Wang, Ying-Hao Liu, Wei-Bing Shuang

Abstract readCase Reports
In one paragraph

Article in World journal of clinical cases, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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0citing papers in PubMed
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1 · What the graph read from it

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The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

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3 · Its place in the literature

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0 citing papers in PubMed.

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4 · The record

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5 · Who and what money

Authors and funding

3 authors.

Yi-Kai WangDepartment of Urology, The First Hospital of Shanxi Medical University, Taiyuan 030001, Shanxi Province, China.
Ying-Hao LiuDepartment of Urology, The First Hospital of Shanxi Medical University, Taiyuan 030001, Shanxi Province, China.
Wei-Bing ShuangDepartment of Urology, The First Hospital of Shanxi Medical University, Taiyuan 030001, Shanxi Province, China. shuangweibing@126.com.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundHemolymphangioma 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.

conclusionThis 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.

Indexed as

Case reportHemolymphangiomaMagnetic resonance imagingRetroperitoneal tumorSurgical excision

Identifiers

PMID39109033
PMCPMC11238797

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.