Two cases of primary solitary fibrous tumor in the pelvis resected using laparoscopic surgery.

Fusion gene Laparoscopic surgery Pelvic tumor STAT6 Solitary fibrous tumor

Journal

International journal of surgery case reports
ISSN: 2210-2612
Titre abrégé: Int J Surg Case Rep
Pays: Netherlands
ID NLM: 101529872

Informations de publication

Date de publication:
2020
Historique:
received: 03 03 2020
revised: 19 04 2020
accepted: 19 04 2020
pubmed: 23 5 2020
medline: 23 5 2020
entrez: 23 5 2020
Statut: ppublish

Résumé

We report two resected cases of solitary fibrous tumors (SFT) that were accidentally found in the pelvic cavity. Case 1 was a 54-year-old male. A colonoscopy for the examination of intestinal polyps revealed an extramural tumor in the right anterior wall of the low rectum. A preoperative MRI showed a well-demarcated T1 low and T2 mixed intensity extramural tumor (53 × 36 mm) located right lateral to the low rectum and behind the seminal vesicle. Laparoscopic surgery was successful for tumor extirpation. Immunohistochemical examination of the specimen revealed STAT6 (+) and CD34 (+) cells, a Ki67 positivity of 7-8%, a mitotic index of 4-5/50 HPF, and a diagnosis of SFT. There was no recurrence 29 months after surgery. Using RT-PCR and sequencing, we detected the NAB2-STAT6 fusion gene but the locus of genomic inversion was not detected. Case 2 was a 43-year-old male that received conservative treatment for appendicitis. A CT scan accidentally revealed a tumor of 40 mm of length in the left obturator area. A MRI revealed a well-demarcated T1 and T2 high intensity tumor. The patient underwent surgical biopsy. Immunohistochemical examination of the biopsy revealed STAT6 (+) and CD34 (+) cells, Ki67 positive cells < 1%, and a diagnosis of SFT. We could not detect the NAB2-STAT6 fusion gene in the extirpated tumor. Two cases of pelvic SFT were diagnosed by immunohistochemical examination, RT-PCR and sequencing and successfully resected by laparoscopic surgery.

Sections du résumé

BACKGROUND BACKGROUND
We report two resected cases of solitary fibrous tumors (SFT) that were accidentally found in the pelvic cavity.
CASE PRESENTATION METHODS
Case 1 was a 54-year-old male. A colonoscopy for the examination of intestinal polyps revealed an extramural tumor in the right anterior wall of the low rectum. A preoperative MRI showed a well-demarcated T1 low and T2 mixed intensity extramural tumor (53 × 36 mm) located right lateral to the low rectum and behind the seminal vesicle. Laparoscopic surgery was successful for tumor extirpation. Immunohistochemical examination of the specimen revealed STAT6 (+) and CD34 (+) cells, a Ki67 positivity of 7-8%, a mitotic index of 4-5/50 HPF, and a diagnosis of SFT. There was no recurrence 29 months after surgery. Using RT-PCR and sequencing, we detected the NAB2-STAT6 fusion gene but the locus of genomic inversion was not detected. Case 2 was a 43-year-old male that received conservative treatment for appendicitis. A CT scan accidentally revealed a tumor of 40 mm of length in the left obturator area. A MRI revealed a well-demarcated T1 and T2 high intensity tumor. The patient underwent surgical biopsy. Immunohistochemical examination of the biopsy revealed STAT6 (+) and CD34 (+) cells, Ki67 positive cells < 1%, and a diagnosis of SFT. We could not detect the NAB2-STAT6 fusion gene in the extirpated tumor.
CONCLUSIONS CONCLUSIONS
Two cases of pelvic SFT were diagnosed by immunohistochemical examination, RT-PCR and sequencing and successfully resected by laparoscopic surgery.

Identifiants

pubmed: 32442915
pii: S2210-2612(20)30273-X
doi: 10.1016/j.ijscr.2020.04.079
pmc: PMC7240175
pii:
doi:

Types de publication

Case Reports

Langues

eng

Pagination

58-65

Informations de copyright

Copyright © 2020 The Author(s). Published by Elsevier Ltd.. All rights reserved.

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Auteurs

Yuki Matsui (Y)

Division of Gastrointestinal Surgery, Kansai Medical University Hospital, Hirakata, Osaka, Japan.

Madoka Hamada (M)

Division of Gastrointestinal Surgery, Kansai Medical University Hospital, Hirakata, Osaka, Japan. Electronic address: hamadamd@hirakata.kmu.ac.jp.

Fusao Sumiyama (F)

Division of Gastrointestinal Surgery, Kansai Medical University Hospital, Hirakata, Osaka, Japan.

Toshinori Kobayashi (T)

Division of Gastrointestinal Surgery, Kansai Medical University Hospital, Hirakata, Osaka, Japan.

Yuki Matsumi (Y)

Division of Gastrointestinal Surgery, Kansai Medical University Hospital, Hirakata, Osaka, Japan.

Hisanori Miki (H)

Division of Gastrointestinal Surgery, Kansai Medical University Hospital, Hirakata, Osaka, Japan.

Mitsuaki Ishida (M)

Department of Pathology and Laboratory Medicine, Kansai Medical University Hospital, Hirakata, Osaka, Japan.

Hiroaki Kurokawa (H)

Department of Radiology, Kansai Medical University Hospital, Hirakata, Osaka, Japan.

Mitsugu Sekimoto (M)

Division of Gastrointestinal Surgery, Kansai Medical University Hospital, Hirakata, Osaka, Japan.

Yoko Sekita-Hatakeyama (Y)

Department of Diagnostic Pathology, Nara Medical University, Kashihara, Nara, Japan.

Kinta Hatakeyama (K)

Department of Diagnostic Pathology, Nara Medical University, Kashihara, Nara, Japan.

Chiho Ohbayashi (C)

Department of Diagnostic Pathology, Nara Medical University, Kashihara, Nara, Japan.

Classifications MeSH