Evidence map›Paper›PMID 36157651›Full record

ArticleWorld journal of clinical cases2022

Renal cell carcinoma presented with a rare case of icteric Stauffer syndrome: A case report.

Dimitar R Popov, Krasimir A Antonov, Evelina G Atanasova, Christo P Pentchev, Lyuben M Milatchkov, Maria D Petkova, Krasimir G Neykov, Rosen K Nikolov

Abstract readCase Reports
In one paragraph

Article in World journal of clinical cases, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

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

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3 · Its place in the literature

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1 citing paper in PubMed.

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4 · The record

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5 · Who and what money

Authors and funding

8 authors.

Dimitar R PopovMedical University of Sofia, Sofia 1431, Bulgaria.
Krasimir A AntonovMedical University of Sofia, Sofia 1431, Bulgaria.
Evelina G AtanasovaClinic of Gastroenterology, University Hospital 'St. Ivan Rilski', Sofia 1431, Bulgaria. eva_gatanasova@abv.bg.
Christo P PentchevMedical University of Sofia, Sofia 1431, Bulgaria.
Lyuben M MilatchkovClinic of Gastroenterology, University Hospital 'St. Ivan Rilski', Sofia 1431, Bulgaria.
Maria D PetkovaMedical University of Sofia, Sofia 1431, Bulgaria.
Krasimir G NeykovClinic of Urology, National Oncology Hospital, Sofia 1756, Bulgaria.
Rosen K NikolovMedical University of Sofia, Sofia 1431, Bulgaria.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundParaneoplastic syndromes remain poorly understood and manifest as multifaceted clinical symptoms, making their diagnosis difficult. Cholestasis can be observed in various malignancies. In rare cases, it can be a paraneoplastic manifestation, most often associated with renal cell carcinoma and other urogenital tumors, as well as with bronchial carcinoma. The classical form of Stauffer syndrome presents with a reversible anicteric increase of cholestatic liver function tests, thrombocytosis, coagulation impairment, and hepatosplenomegaly, without any proven hepatobiliary obstruction or metastases. CASE SUMMARY: We report a patient who presented with elevated liver enzymes, cholestatic jaundice, weight loss and pruritus, in whom renal cell carcinoma was incidentally found during hospitalization. Clinical, laboratory, and imaging tests excluded primary hepatic cause or metastatic disease. Jaundice and laboratory abnormalities reversed completely a few months after nephrectomy. This case is an example of the many sides of renal cell carcinoma, and it focuses the clinicians' attention on the differential diagnosis of cholestasis, including Stauffer syndrome and its variant. Thus, the correct diagnosis can be straightforward and the associated malignancy can be treated promptly. All cases should be followed up with a multidisciplinary team. Interleukin (IL)-6 is proposed to contribute to the pathophysiology of the condition. The probable mechanism is proinflammatory activity by the IL-6 cytokine, causing elevation of C-reactive protein and haptoglobin and inhibition of hepatobiliary transporter gene expression, impairing biliary outflow.

conclusionDespite being rare, Stauffer syndrome is a potentially reversible paraneoplastic condition, when the primary cause is treatable. This syndrome should be considered by clinicians because of the remediable liver disturbance, after successful treatment of the underlying malignancy.

Indexed as

Case reportCholestasisJaundiceRenal cell carcinomaStauffer syndrome

Identifiers

PMID36157651
PMCPMC9477025

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