Evidence map›Paper›PMID 33457201›Full record

ArticleRespiratory medicine case reports2021

Systemic sarcoidosis mimicking metastatic renal cell carcinoma with subsequent cardiac involvement.

Michael Frohlich, Najwa Buhlaiga, Hangjun Wang, Francois Patenaude, Christian Sirois, Lama Sakr

Abstract readCase Reports
In one paragraph

Article in Respiratory medicine case reports, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

0numbers the graph read from it
0cells of the map it votes in
0citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

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.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

0 citing papers in PubMed.

No citing paper in PubMed yet.

4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

6 authors.

Michael FrohlichDepartment of Medicine, Division of Pulmonary Disease, Jewish General Hospital, Pavilion G Room 203, 3755 Côte-Sainte-Catherine Road, Montreal, Quebec, H3T 1E2, Canada.
Najwa BuhlaigaDepartment of Medicine, Hematology Service and Department of Oncology, Jewish General Hospital, Pavilion E7, 3755 Côte-Sainte-Catherine Road, Montreal, Quebec, H3T 1E2, Canada.
Hangjun WangDivisions of Pathology and Molecular Genetics, Jewish General Hospital, Pavillion G Room 108, 3755 Côte-Sainte-Catherine Road, Montreal, Quebec, H3T 1E2, Canada.
Francois PatenaudeDepartment of Medicine, Hematology Service and Department of Oncology, Jewish General Hospital, Pavilion E7, 3755 Côte-Sainte-Catherine Road, Montreal, Quebec, H3T 1E2, Canada.
Christian SiroisDepartment of Surgery, Division Thoracic and Upper Gastrointestinal Surgery, Montreal General Hospital, Pavilion L Room 8-505, 1650 Cedar Avenue, Montreal, Quebec, H3G 1A4, Canada.
Lama SakrDepartment of Medicine, Division of Pulmonary Disease, Jewish General Hospital, Pavilion G Room 203, 3755 Côte-Sainte-Catherine Road, Montreal, Quebec, H3T 1E2, Canada.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

There exists a well-established association between sarcoidosis and many solid and hematologic malignancies however it is a less frequently described phenomenon in patients with renal cell carcinoma. Moreover the majority of described cases presented with local sarcoid-like reactions in close proximity to the tumor with comparatively few reports of more distant disease. Given the relatively low number of cases there remains a great deal of uncertainty surrounding the clinical behaviour of sarcoidosis in the setting of renal cell carcinoma. We report the case of a patient with surgically resected renal cell carcinoma who, several years later, developed bilateral pulmonary nodules, intra-thoracic lymphadenopathy as well as splenic, hepatic and osseous lesions. After extensive investigation, culminating in video-assisted thoracoscopic surgical resection, he was found to have sarcoidosis. He remained asymptomatic for many years before being diagnosed with cardiac sarcoidosis, which was found to be inactive and did not require any treatment. Both his sarcoidosis and underlying renal cell carcinoma have remained in remission to date. This case highlights the variable behaviour of sarcoidosis in these patients and underscores the importance of obtaining an accurate tissue diagnosis in the setting of suspected metastatic disease. Additionally, it underscores the importance of close monitoring and long-term follow up as these patients may develop significant organ involvement, even many years after diagnosis. Interestingly the patient's renal cell carcinoma remained in remission, raising questions about whether the development of sarcoidosis portends a better prognosis in patients with an underlying solid malignancy.

Indexed as

CancerCT, computed tomographyEBUS-TBNA, endobronchial ultrasound-guided transbronchial needle aspirationEndobronchial ultrasoundIFN- γ, interferon γIL, interleukinMRI, magnetic resonance imagingPET, positron emission tomographyRCC, renal cell carcinomaRenal cell carcinomaSarcoidosisTh17, T-helper cell type 17Th1, T-helper cell type 1TTNA, transthoracic-needle aspiration

Identifiers

PMID33457201
PMCPMC7797905

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC-ND
Read underepoch 390

Registered trials

None linked

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.