Robotic wedge resection of a rare gastric perivascular epithelioid cell tumor: A case report.

Case report Minimally invasive Perivascular epithelioid cell tumor Robotic Stomach Surgery

Journal

World journal of clinical cases
ISSN: 2307-8960
Titre abrégé: World J Clin Cases
Pays: United States
ID NLM: 101618806

Informations de publication

Date de publication:
06 Dec 2019
Historique:
received: 19 08 2019
revised: 31 10 2019
accepted: 14 11 2019
entrez: 14 12 2019
pubmed: 14 12 2019
medline: 14 12 2019
Statut: ppublish

Résumé

Perivascular epithelioid cell tumor (PEComa) is a rare mesenchymal neoplasm that can arise in many different organs with a broad spectrum of biological behavior, from indolent to aggressive progression. Only ten cases of gastric PEComas have been reported in the English literature, which were treated with endoscopic, laparoscopic, or open resections. Due to its rarity, the optimal surgical management and prognosis of this tumor are still uncertain. We present a case of robotic wedge resection of a 6.5 cm bleeding lesion of the gastric fundus located 3 cm below the esophago-gastric junction in a 55-year-old man. Biopsy revealed a malignant tumor with epithelioid cells focally positive for muscle markers desmin and smooth muscle actin. In addition, histology revealed that the tumor was positive for HMB-45, melan-A (MART-1), microphthalmia transcription factor and negative for pan-cytokeratin AE1/AE3, CD34, p40, DOG-1, CD117 (c-kit), S100, CD3, CD79a, caldesmon and myogenin. These markers suggested the possibility of a PEComa. The patient underwent a diagnostic laparoscopy Gastric PEComa can be treated with a robotic R0 resection with acceptable postoperative and short-term oncological outcomes.

Sections du résumé

BACKGROUND BACKGROUND
Perivascular epithelioid cell tumor (PEComa) is a rare mesenchymal neoplasm that can arise in many different organs with a broad spectrum of biological behavior, from indolent to aggressive progression. Only ten cases of gastric PEComas have been reported in the English literature, which were treated with endoscopic, laparoscopic, or open resections. Due to its rarity, the optimal surgical management and prognosis of this tumor are still uncertain.
CASE SUMMARY METHODS
We present a case of robotic wedge resection of a 6.5 cm bleeding lesion of the gastric fundus located 3 cm below the esophago-gastric junction in a 55-year-old man. Biopsy revealed a malignant tumor with epithelioid cells focally positive for muscle markers desmin and smooth muscle actin. In addition, histology revealed that the tumor was positive for HMB-45, melan-A (MART-1), microphthalmia transcription factor and negative for pan-cytokeratin AE1/AE3, CD34, p40, DOG-1, CD117 (c-kit), S100, CD3, CD79a, caldesmon and myogenin. These markers suggested the possibility of a PEComa. The patient underwent a diagnostic laparoscopy
CONCLUSION CONCLUSIONS
Gastric PEComa can be treated with a robotic R0 resection with acceptable postoperative and short-term oncological outcomes.

Identifiants

pubmed: 31832403
doi: 10.12998/wjcc.v7.i23.4011
pmc: PMC6906564
doi:

Types de publication

Case Reports

Langues

eng

Pagination

4011-4019

Informations de copyright

©The Author(s) 2019. Published by Baishideng Publishing Group Inc. All rights reserved.

Déclaration de conflit d'intérêts

Conflict-of-interest statement: The authors declare that they have no conflict of interest.

Références

J Clin Oncol. 2010 Feb 10;28(5):835-40
pubmed: 20048174
AJR Am J Roentgenol. 2007 Aug;189(2):299-305
pubmed: 17646454
Histopathology. 2006 Jan;48(1):75-82
pubmed: 16359539
J Pathol Transl Med. 2017 Jul;51(4):428-432
pubmed: 28372349
Gastroenterology. 2017 Aug;153(2):357-359
pubmed: 28672123
Surg Laparosc Endosc Percutan Tech. 2018 Feb;28(1):e1-e7
pubmed: 29215507
Surg Endosc. 2011 Dec;25(12):3939-45
pubmed: 21656069
Sarcoma. 2012;2012:541626
pubmed: 22619565
Int J Surg Case Rep. 2012;3(2):89-91
pubmed: 22288055
World J Gastroenterol. 2015 Jan 28;21(4):1349-56
pubmed: 25632212
Clin Radiol. 2013 Jun;68(6):555-61
pubmed: 23245276
Am J Surg Pathol. 2013 Dec;37(12):1769-82
pubmed: 24061520
Arch Surg. 2003 Jul;138(7):777-84
pubmed: 12860761
World J Gastroenterol. 2010 Jan 28;16(4):522-5
pubmed: 20101783
Adv Anat Pathol. 2008 Mar;15(2):63-75
pubmed: 18418088
Am J Surg Pathol. 2005 Dec;29(12):1558-75
pubmed: 16327428
Diagn Pathol. 2013 Apr 15;8:60
pubmed: 23587410
Medicine (Baltimore). 2016 Jul;95(28):e3890
pubmed: 27428182
Am J Surg Pathol. 2000 Sep;24(9):1239-46
pubmed: 10976698

Auteurs

Alessandra Marano (A)

Department of Surgery, General and Oncologic Surgery Unit, Santa Croce e Carle Hospital, Cuneo 12100, Italy.

Francesca Maione (F)

Department of Surgery, General and Oncologic Surgery Unit, Santa Croce e Carle Hospital, Cuneo 12100, Italy.

Yanghee Woo (Y)

Department of Surgery, City of Hope, Duarte, CA 91010, United States.

Luca Pellegrino (L)

Department of Surgery, General and Oncologic Surgery Unit, Santa Croce e Carle Hospital, Cuneo 12100, Italy.

Paolo Geretto (P)

Department of Surgery, General and Oncologic Surgery Unit, Santa Croce e Carle Hospital, Cuneo 12100, Italy.

Diego Sasia (D)

Department of Surgery, General and Oncologic Surgery Unit, Santa Croce e Carle Hospital, Cuneo 12100, Italy.

Mirella Fortunato (M)

Department of Pathology, Santa Croce e Carle Hospital, Cuneo 12100, Italy.

Giulio Fraternali Orcioni (GF)

Department of Pathology, Santa Croce e Carle Hospital, Cuneo 12100, Italy.

Roberto Priotto (R)

Department of Radiology, Santa Croce e Carle Hospital, Cuneo 12100, Italy.

Renato Fasoli (R)

Department of Gastroenterology and Digestive Endoscopy, Santa Croce e Carle Hospital, Cuneo 12100, Italy.

Felice Borghi (F)

Department of Surgery, General and Oncologic Surgery Unit, Santa Croce e Carle Hospital, Cuneo 12100, Italy. borghi.f@ospedale.cuneo.it.

Classifications MeSH