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1.
Clin J Gastroenterol ; 15(2): 351-357, 2022 Apr.
Article in English | MEDLINE | ID: mdl-34993902

ABSTRACT

Endoscopic stenting is useful for amelioration of gastrointestinal stenosis. This procedure benefits severely compromised patients who cannot afford surgery. Although the self-expandable metallic stent (SEMS) is safe, it is also associated with several complications such as perforation, migration, and fracture. Migration of a SEMS is not particularly rare; however, fracture of a SEMS is relatively rare. An 88-year-old man underwent stenting for dysphagia at another hospital. He was being treated for gastric cancer at the esophagogastric junction. After appropriate stenting, he regained his ability to eat and was discharged the hospital. Only 2 months later, however, he again lost his ability to eat and visited our hospital. Abdominal X-ray and computed tomography revealed a stent fracture. The proximal fragment was in the esophagus, and the distal fragment was in the stomach. An emergency operation involving gastrotomy and gastrostomy was performed. Open gastrotomy was performed to remove the fractured distal stent, and percutaneous tube gastrostomy was placed through the same gastric incision for nutrition support. The surgery was successful, and he was again able to eat. In this report, we discuss the occurrence of SEMS fracture within a short time periods after insertion.


Subject(s)
Self Expandable Metallic Stents , Stomach Neoplasms , Aged, 80 and over , Esophagogastric Junction/surgery , Gastrectomy , Humans , Male , Retrospective Studies , Stents , Stomach Neoplasms/complications , Stomach Neoplasms/surgery , Treatment Outcome
2.
Gan To Kagaku Ryoho ; 35(3): 507-9, 2008 Mar.
Article in Japanese | MEDLINE | ID: mdl-18347406

ABSTRACT

A sixty-year-old man was admitted with anorexia and abdominal mass. Colonoscopy revealed type 2 tumor at sigmoid colon. Computed tomography (CT) demonstrated multiple liver metastases. The patient was diagnosed as sigmoid colon cancer with multiple liver metastases. The patient was treated with mFOLFOX6 as neoadjuvant chemotherapy because the liver metastases were unresectable. However, after 2 cycles of mFOLFOX6, the level of CEA and CA19-9 much increased. The regimen was replaced by FOLFIRI. The level of CEA and CA19-9 decreased after 2 cycles of FOLFIRI. CEA and CA19-9 further decreased and colonoscopy and CT revealed a partial response after 5 cycles of FOLFIRI. The patient was subjected to curative resection. Sigmoidectomy and liver resection were performed. Histological response was Grade 1b at liver metastasis. The patient was discharged and had an uneventful recovery. Six months after surgery, CEA and CA19-9 decreased to normal level, and the patient is free of recurrence. Neoadjuvant chemotherapy for metastatic colorectal cancer may render some unresectable patients resectable, affording these patients the possibility of prolonged survival. However, the optimal approach is unknown.


Subject(s)
Antineoplastic Combined Chemotherapy Protocols/therapeutic use , Colorectal Neoplasms/drug therapy , Liver Neoplasms/drug therapy , Liver Neoplasms/secondary , Biomarkers, Tumor/blood , Camptothecin/analogs & derivatives , Camptothecin/therapeutic use , Colonoscopy , Colorectal Neoplasms/blood , Colorectal Neoplasms/pathology , Colorectal Neoplasms/surgery , Fluorouracil/therapeutic use , Humans , Leucovorin/therapeutic use , Liver Neoplasms/pathology , Liver Neoplasms/surgery , Male , Middle Aged , Organoplatinum Compounds/therapeutic use , Time Factors , Tomography, X-Ray Computed , Treatment Failure
5.
J Pediatr Surg ; 38(7): 1099-101, 2003 Jul.
Article in English | MEDLINE | ID: mdl-12861550

ABSTRACT

A congenital midline cervical cleft (CMCC) is a rare developmental anomaly. It may represent failure of the branchial arches to fuse in the midline and presents at birth with a ventral midline defect of the skin of the neck. Congenital heart disease along with CMCC is rarer, and most of the cases reported are associated with chest wall defects or thoracic ectopia cordis. The authors report a case of a 5-month-old girl with CMCC and an atrial septal defect (ASD) and discuss the clinical presentation, embryologic development, and treatment.


Subject(s)
Neck/abnormalities , Neck/surgery , Abnormalities, Multiple , Female , Heart Septal Defects, Atrial/complications , Humans , Infant , Plastic Surgery Procedures
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