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Multiple calcifying fibrous tumors from gastric and retroperitoneal tissue: A case report.
Ishii, Masatsugu; Nitta, Toshikatsu; Taki, Masataka; Kubo, Ryutaro; Takeshita, Atsushi; Ishibashi, Takashi.
Afiliación
  • Ishii M; Division of Surgery Gastroenterological Center, Medico Shunju Shiroyama Hospital, Habikino, Japan. Electronic address: masatsu@hotmail.co.jp.
  • Nitta T; Division of Surgery Gastroenterological Center, Medico Shunju Shiroyama Hospital, Habikino, Japan.
  • Taki M; Division of Surgery Gastroenterological Center, Medico Shunju Shiroyama Hospital, Habikino, Japan.
  • Kubo R; Division of Surgery Gastroenterological Center, Medico Shunju Shiroyama Hospital, Habikino, Japan.
  • Takeshita A; Department of Diagnostic Pathology, Osaka Medical and Pharmaceutical College Hospital, 2-7 Daigaku-machi, Takatsuki City, Osaka 569-8686, Japan.
  • Ishibashi T; Division of Surgery Gastroenterological Center, Medico Shunju Shiroyama Hospital, Habikino, Japan.
Int J Surg Case Rep ; 121: 109944, 2024 Aug.
Article en En | MEDLINE | ID: mdl-39024990
ABSTRACT
INTRODUCTION AND IMPORTANCE Calcifying fibrous tumor (CFT) is a rare benign mesenchymal lesion that has been occurred in the gastrointestinal tract, especially occurs most commonly in the stomach and the small and large intestines. CASE PRESENTATION 74-year-old woman was admitted to our hospital with complaints of epigastric discomfort. Whole-body computed tomography (CT) revealed a 2.2-cm mass with a 1.2-cm low-density area at the anterior wall in the gastric cardia and lesser omentum; however, no abnormal uptake at the same site was noted on positron emission tomography (PET). We performed laparoscopic tumor resection of the two sites. The postoperative course was good without complications. Histopathological findings revealed collagen fibrous granulation connective tissue and psammomatous calcification. Subsequently, the patient has been relapse-free for 6 months. CLINICAL

DISCUSSION:

CFT is a rare benign tumor that commonly occurs in soft tissues, such as the subcutaneous extremities and neck. In particular, development from the stomach and lesser omentum has never been reported. Our case was incidentally found on a general examination. In our case, CT showed a low-density area, MRI showed a low-intensity area, and PET examination showed no uptake; it was difficult to establish a preoperative diagnosis. Therefore, in our case, laparoscopic tumor resection was performed, with GIST as the differential diagnosis.

CONCLUSIONS:

We herein reported a rare gastric and lesser omentum CFT that was successfully treated by laparoscopic surgery. For curative treatment of CFT, complete surgical resection is necessary.
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Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Idioma: En Revista: Int J Surg Case Rep Año: 2024 Tipo del documento: Article

Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Idioma: En Revista: Int J Surg Case Rep Año: 2024 Tipo del documento: Article
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