Evidence map›Paper›PMID 35620211›Full record

ArticleMolecular and clinical oncology2022

A successful operation for giant intra-abdominal desmoid tumors associated with familial adenomatous polyposis: A case report.

Yoshitoshi Ichikawa, Kyowon Lee, Takashi Yokouchi, Souta Watanabe, Daishi Yoshimura, Gaku Mizojiri, Kentaro Maruyama, Tamaki Maeda, Yasushi Fujimori, Hiroshi Oka

Open access · diamondAbstract readCase Reports
In one paragraph

Article in Molecular and clinical oncology, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.

0numbers the graph read from it
0cells of the map it votes in
2citing papers in PubMed
0.3field-weighted citation impact, top 41% 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

2 citing papers in PubMed, 2 citations in OpenAlex.

  1. Article
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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 1 institution in 1 country.

Yoshitoshi IchikawaDepartment of Surgery, Moriguchi Keijinkai Hospital, Moriguchi, Osaka 570-0021, Japan.
Kyowon LeeDepartment of Surgery, Moriguchi Keijinkai Hospital, Moriguchi, Osaka 570-0021, Japan.
Takashi YokouchiDepartment of Surgery, Moriguchi Keijinkai Hospital, Moriguchi, Osaka 570-0021, Japan.
Souta WatanabeDepartment of Surgery, Moriguchi Keijinkai Hospital, Moriguchi, Osaka 570-0021, Japan.
Daishi YoshimuraDepartment of Surgery, Moriguchi Keijinkai Hospital, Moriguchi, Osaka 570-0021, Japan.
Gaku MizojiriDepartment of Surgery, Moriguchi Keijinkai Hospital, Moriguchi, Osaka 570-0021, Japan.
Kentaro MaruyamaDepartment of Surgery, Moriguchi Keijinkai Hospital, Moriguchi, Osaka 570-0021, Japan.
Tamaki MaedaDepartment of Pathology, Moriguchi Keijinkai Hospital, Moriguchi, Osaka 570-0021, Japan.
Yasushi FujimoriDepartment of Plastic Surgery, Moriguchi Keijinkai Hospital, Moriguchi, Osaka 570-0021, Japan.
Hiroshi OkaDepartment of Surgery, Moriguchi Keijinkai Hospital, Moriguchi, Osaka 570-0021, Japan.
Teine Keijinkai Hospital · JP

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Desmoid tumors are benign proliferations of spindle cells originating in fibro-aponeurotic tissue. Many patients with familial adenomatous polyposis (FAP) die from desmoid tumors, which can arise spontaneously but often appear to be surgically induced by prophylactic colectomy. Desmoid tumors are the second most common cause of death in patients with FAP, second to colorectal cancer. Many patients can live a long life with desmoid tumors without symptoms, but when symptoms (ranging from bowel or ureteric obstruction to bowel perforation with abscess and fistula) appear or there is a risk of functional impairment, a wide spectrum of therapies (local and systemic) are valuable in improving the symptoms and controlling the disease. A half-Japanese, half-Caucasian male, who had been diagnosed with intra-abdominal desmoid tumors associated with FAP at age 13, was treated using abdominal wall incision for decompression and chemotherapy from the age of 38. The therapeutic outcome was progressive disease, based on the modified response evaluation criteria in solid tumors (mRECIST), and when he visited our hospital at age 41 the desmoid tumor had invaded the small bowel with a fistula to the abdominal wall. We performed a palliative operation to improve his symptoms, which were fever, abdominal pain, vomiting, and difficulty eating. As the tumor was extremely large and had invaded the small intestine, massive resection including the small intestine was required. To prepare for anticipated massive bleeding, a balloon catheter was placed in the superior mesenteric artery just prior to surgery. Although the operation was extremely difficult, following surgery the patient regained his ability to eat and when discharged was ambulatory and without short-bowel syndrome. We report our experience treating one of the largest reported intraperitoneal desmoid tumors. Resection resulted in a good postoperative course, with improved quality of life and prognosis.

Indexed as

APC genedesmoid tumorfamilial adenomatous polyposisgiant mesenteric tumorhereditary colorectal cancer

Identifiers

PMID35620211
PMCPMC9112404
OpenAlexW4229067861

What OpenQuestion holds

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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.