Endoscopy 2019; 51(04): S256
DOI: 10.1055/s-0039-1681944
ESGE Days 2019 ePosters
Friday, April 5, 2019 09:00 – 17:00: Stomach and small intestine ePosters
Georg Thieme Verlag KG Stuttgart · New York

A RHABDOID CAVITATED JEJUNAL ADENOCARCINOMA DIAGNOSED BY DOUBLE-BALLOON ASSISTED ENTEROSCOPY

A Pérez Fernandez
1   Morales Meseguer Hospital, Small Bowel Unit, Murcia, Spain
,
E Pérez-Cuadrado-Robles
2   Cliniques Universitaires Saint-Luc, Endoscopy Unit, Gastroenterology, Brussels, Belgium
,
J Francisco Sánchez Melgarejo
1   Morales Meseguer Hospital, Small Bowel Unit, Murcia, Spain
,
JM Rubio Mateos
1   Morales Meseguer Hospital, Small Bowel Unit, Murcia, Spain
,
M José Sánchez Fernandez
1   Morales Meseguer Hospital, Small Bowel Unit, Murcia, Spain
,
P Esteban Delgado
1   Morales Meseguer Hospital, Small Bowel Unit, Murcia, Spain
,
JL Rodrigo Agudo
1   Morales Meseguer Hospital, Small Bowel Unit, Murcia, Spain
,
E Pérez-Cuadrado Martínez
1   Morales Meseguer Hospital, Small Bowel Unit, Murcia, Spain
› Author Affiliations
Further Information

Publication History

Publication Date:
18 March 2019 (online)

 

Introduction:

The rhabdoid phenotypic characteristic in digestive tumors is exceptional. In the jejunum, the primitive undifferentiated adenocarcinoma rarely grows up to invade other organs and appears as a cavitated mass.

Case report:

A 64 years-old patient with multifactorial anemia and transfusional requirements underwent a normal gastroscopy and colonoscopy. This last procedure confirmed a 2 cm flat lesion in the right colon and the histopathological analysis reported adenocarcinoma.

Furthermore, a CT confirmed a mass dependent of small bowel and a PET-CT reported mesenteric implants with an extension on both adrenal glands and swollen lymph nodes. The biopsy of a peripheral adenopathy was an undifferentiated adenocarcinoma.

Thus, an oral double-balloon enteroscopy was performed. The procedure showed a large cavitated mass in jejunum consisting of a very irregular mucous membrane with proliferative, necrotic areas and diffuse as well as a ongoing mild-bleeding. Biopsies were taken. The enteroscope could assess the mass intracavitary, in retroversion, and the "outcoming" inside of the small bowel was visualized.

Finally, an undifferentiated rhabdoid carcinoma (vimentin, CKae1-be3 +) was confirmed by the histopathological analysis, excluding GIST or neural origin. The CT ruled out pneumoperitoneum, showing peritoneal and pleural neoplastic progression. Subsequent pathologic study of all samples of the various organs gave similar results. The patient was treated by chemotherapy.

Conclusions:

Small bowel undifferentiated rhabdoid carcinoma is rare, with a great aggressiveness and bad prognosis. At this location, there are only 11 cases described, almost the half of them in the jejunum. This case has affected other organs (including colon) with multiorgan metastases. Endoscopically, a big and cavitated jejunal is also a rarity, only described in eccentrics GIST. There are no previous publications describind this entity by flexible enteroscopy.