Evidence map›Paper›PMID 31713159›Full record

ArticleClinical journal of gastroenterology2020

A rare case of peliosis hepatis in a patient with chronic renal failure and renal cell carcinoma.

Hiroki Maruyama, Kazuya Takahashi, Natsuki Ishikawa, Kazunori Hosaka, Daisuke Kumaki, Yukio Aruga, Masashi Yamakawa, Masaaki Hirano, Kazuhiro Funakoshi, Shuji Terai

Abstract readCase Reports
PubMed Publisher
In one paragraph

Article in Clinical journal of gastroenterology, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 3 papers.

0numbers the graph read from it
0cells of the map it votes in
3citing papers in PubMed
0.3field-weighted citation impact, top 42% of its field
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

3 citing papers in PubMed, 6 citations in OpenAlex.

  1. Hepatic peliosis in a newborn - A case report and review of the literature.International journal of surgery case reports · 2024
    Article
  2. Article
  3. Article
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

10 authors at 2 institutions in 1 country.

Hiroki MaruyamaDepartment of Internal Medicine, Niigata Prefectural Central Hospital, 205 Shinnancho, Joetsu City, 943-0192, Niigata, Japan.
Kazuya TakahashiDepartment of Internal Medicine, Niigata Prefectural Central Hospital, 205 Shinnancho, Joetsu City, 943-0192, Niigata, Japan. kazuya911@med.niigata-u.ac.jp.ORCID http://orcid.org/0000-0002-3097-9841
Natsuki IshikawaDepartment of Internal Medicine, Niigata Prefectural Central Hospital, 205 Shinnancho, Joetsu City, 943-0192, Niigata, Japan.
Kazunori HosakaDepartment of Internal Medicine, Niigata Prefectural Central Hospital, 205 Shinnancho, Joetsu City, 943-0192, Niigata, Japan.
Daisuke KumakiDepartment of Internal Medicine, Niigata Prefectural Central Hospital, 205 Shinnancho, Joetsu City, 943-0192, Niigata, Japan.
Yukio ArugaDepartment of Internal Medicine, Niigata Prefectural Central Hospital, 205 Shinnancho, Joetsu City, 943-0192, Niigata, Japan.
Masashi YamakawaDepartment of Internal Medicine, Niigata Prefectural Central Hospital, 205 Shinnancho, Joetsu City, 943-0192, Niigata, Japan.
Masaaki HiranoDepartment of Internal Medicine, Niigata Prefectural Central Hospital, 205 Shinnancho, Joetsu City, 943-0192, Niigata, Japan.
Kazuhiro FunakoshiDepartment of Internal Medicine, Niigata Prefectural Central Hospital, 205 Shinnancho, Joetsu City, 943-0192, Niigata, Japan.
Shuji TeraiDivision of Gastroenterology and Hepatology, Graduate School of Medical and Dental Sciences, Niigata University, 1-757 Asahimachi-dori, Chuo-ku, Niigata City, 951-8510, Niigata, Japan.
Niigata Prefectural Central Hospital · JPNiigata University Medical and Dental Hospital · JP

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Peliosis hepatis (PH) is a rare disease characterized by the presence of sinusoidal dilation and blood-filled cysts throughout the hepatic parenchyma. We report a case of PH in a 49-year-old woman with chronic renal failure (CRF) on hemodialysis and with renal cell carcinoma (RCC). Dynamic contrast-enhanced computed tomography (CT) showed a 35-mm-diameter, hypervascular tumor in the liver and RCC in the right renal cyst. Ultrasound and superparamagnetic iron oxide-enhanced magnetic resonance imaging were also performed; however, the liver tumor could not be distinguished from the metastasis of RCC. Therefore, echo-guided biopsy of the liver tumor using an 18-G Majima needle was performed. Histological evaluation of the specimen showed irregular sinusoidal dilatation and blood-filled cavities without malignant cells. She was ultimately diagnosed with PH. Subsequently, she underwent total right nephrectomy for RCC and was diagnosed with RCC stage 1 (pT1N0M0). A follow-up CT performed 4 months after nephrectomy showed no growth of PH. Although the development of PH in patients with CRF or RCC who do not undergo renal transplantation is extremely rare, it should be considered in the differential diagnosis to distinguish PH from the metastasis of RCC.

Indexed as

Biopsy, NeedleCarcinoma, Renal CellFemaleHumansKidney Failure, ChronicKidney NeoplasmsLiverMiddle AgedPeliosis HepatisTomography, X-Ray ComputedUltrasonographyChronic renal failureHemodialysisPeliosis hepatisRenal cell carcinoma

Identifiers

PMID31713159
OpenAlexW2988611079

What OpenQuestion holds

Textmetadata
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.