Evidence map›Paper›PMID 28420844›Full record

ArticleInternal medicine (Tokyo, Japan)2017

Protein-losing Enteropathy Caused by Intestinal or Colonic Lymphangiectasia Complicated by Sporadic Lymphangioleiomyomatosis: A Report of Two Cases.

Koichi Nishino, Kaku Yoshimi, Tomoyoshi Shibuya, Takuo Hayashi, Keiko Mitani, Etsuko Kobayashi, Masako Ichikawa, Tetsuhiko Asao, Yohei Suzuki, Tadashi Sato and 4 more

Open access · diamondAbstract readCase Reports
In one paragraph

Article in Internal medicine (Tokyo, Japan), 2017. 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
0.3field-weighted citation impact, top 40% 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

0 citing papers in PubMed, 3 citations in OpenAlex.

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

14 authors at 1 institution in 1 country.

Koichi NishinoDivision of Respiratory Medicine, Juntendo University Faculty of Medicine and Graduate School of Medicine, Japan.
Kaku YoshimiDivision of Respiratory Medicine, Juntendo University Faculty of Medicine and Graduate School of Medicine, Japan.
Tomoyoshi ShibuyaDivision of Gastroenterology, Juntendo University Faculty of Medicine and Graduate School of Medicine, Japan.
Takuo HayashiDivision of Human Pathology, Juntendo University Faculty of Medicine and Graduate School of Medicine, Japan.
Keiko MitaniDivision of Human Pathology, Juntendo University Faculty of Medicine and Graduate School of Medicine, Japan.
Etsuko KobayashiDivision of Respiratory Medicine, Juntendo University Faculty of Medicine and Graduate School of Medicine, Japan.
Masako IchikawaDivision of Respiratory Medicine, Juntendo University Faculty of Medicine and Graduate School of Medicine, Japan.
Tetsuhiko AsaoDivision of Respiratory Medicine, Juntendo University Faculty of Medicine and Graduate School of Medicine, Japan.
Yohei SuzukiDivision of Respiratory Medicine, Juntendo University Faculty of Medicine and Graduate School of Medicine, Japan.
Tadashi SatoDivision of Respiratory Medicine, Juntendo University Faculty of Medicine and Graduate School of Medicine, Japan.
Satomi ShiotaDivision of Respiratory Medicine, Juntendo University Faculty of Medicine and Graduate School of Medicine, Japan.
Yuzo KodamaDivision of Respiratory Medicine, Juntendo University Faculty of Medicine and Graduate School of Medicine, Japan.
Kazuhisa TakahashiDivision of Respiratory Medicine, Juntendo University Faculty of Medicine and Graduate School of Medicine, Japan.
Kuniaki SeyamaDivision of Respiratory Medicine, Juntendo University Faculty of Medicine and Graduate School of Medicine, Japan.
Juntendo University · JP

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

This report describes two patients with sporadic lymphangioleiomyomatosis complicated by protein-losing enteropathy (PLE). Imaging studies indicated retroperitoneal lymphangioleiomyomas and abnormalities of the adjacent digestive tract. Endoscopic mucosal biopsy revealed colonic lymphangiectasia in one patient; whereas the site in the other patient was intestinal. Treatment with sirolimus led to the complete resolution of PLE within several months; additionally, marked shrinkage was observed in the lymphangioleiomyomas of both cases. These findings suggest that colonic or intestinal lymphatic congestion due to neighboring lymphangioleiomyomas was the mechanism for the development of PLE. At the time of writing this report, the beneficial effect of sirolimus has lasted for more than 3 years.

Indexed as

AdultColonic DiseasesDiet, Fat-RestrictedDiet TherapyFemaleHumansImmunosuppressive AgentsIntestinal DiseasesLymphangiectasisLymphangioleiomyomatosisProtein-Losing EnteropathiesSirolimusTreatment OutcomeImmunosuppressive AgentsSirolimuscolonic lymphangiectasiaintestinal lymphangiectasialymphangioleiomyomatosisprotein-losing enteropathysirolimus

Identifiers

PMID28420844
PMCPMC5465412
OpenAlexW2605548108

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC-ND
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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.