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1.
BMJ Case Rep ; 17(2)2024 Feb 17.
Article in English | MEDLINE | ID: mdl-38367992

ABSTRACT

Intussusception following Roux-en-Y gastric bypass is a rare, potentially life-threatening complication. Patients present with intermittent obstructive symptoms, and the diagnosis is made on imaging. Treatment is surgical considering the high likelihood of non-operative failure, strangulation, incarceration, perforation and concern for malignancy. We present the case of a woman in her 60s with a history of Roux-en-Y gastric bypass who presented with retrograde jejunojejunal intussusception at the distal Roux anastomosis. She proceeded to the operating room for complete anastomotic resection with reconstruction of three blind ends via two sequential isoperistaltic anastomoses. She progressed appropriately throughout her hospitalisation and was discharged on postoperative day 5 without recurrence. While intussusception in Roux-en-Y anatomy has been previously described, a literature review yielded sparse results in detailing its surgical correction. We highlight our unique surgical approach of jejunojejunal anastomotic resection with the creation of sequential isoperistaltic side-to-side anastomoses.


Subject(s)
Gastric Bypass , Gastrointestinal Diseases , Intussusception , Female , Humans , Anastomosis, Roux-en-Y/adverse effects , Gastric Bypass/adverse effects , Gastrointestinal Diseases/etiology , Intussusception/diagnostic imaging , Intussusception/etiology , Intussusception/surgery , Middle Aged , Aged
2.
Transplantation ; 108(2): 346-356, 2024 Feb 01.
Article in English | MEDLINE | ID: mdl-37271882

ABSTRACT

The impact of bariatric surgery (BS) on kidney transplantation (KT) outcomes in patients with obesity remains controversial. We systematically searched MEDLINE, EMBASE, Scopus, Web of Science, and Cochrane Central Register of Controlled Trials for studies reporting outcomes of KT recipients that underwent prior BS. Common/random effects meta-analyses were performed to obtain summary ratios of the postoperative outcomes. Eighteen eligible studies involving 315 patients were identified. Sleeve gastrectomy was the most common BS type (65.7%) followed by Roux-en-Y gastric bypass (27.6%) and gastric banding (4.4%). Across studies that provided the data, the %excess weight loss from BS to KT was 62.79% (95% confidence interval [CI], 52.01-73.56; range, 46.2%-80.3%). The rates of delayed graft function and acute rejection were 16% (95% CI, 7%-28%) and 16% (95% CI, 11%-23%) in 14 and 11 studies that provided this data, respectively. The rates of wound, urinary, and vascular complications following KT were 5% (95% CI, 0%-13%),19% (95% CI, 2%-42%), and 2% (95% CI, 0%-5%), in 12, 9, and 11 studies that provided this data, respectively. Follow-up time after KT was reported in 11 studies (61.1%) and ranged from 16 mo to >5 y. Graft loss was reported in 14 studies with an average of 3% (95% CI, 1%-6%). Four studies that included a comparator group of patients with obesity who did not undergo BS before KT showed comparable outcomes between the groups. We conclude that currently there is a paucity of robust evidence to suggest that pretransplant BS has a major effect on post-KT outcomes. High-quality studies are needed to fully evaluate the impact of BS on KT outcomes.


Subject(s)
Bariatric Surgery , Gastric Bypass , Kidney Transplantation , Obesity, Morbid , Humans , Kidney Transplantation/adverse effects , Bariatric Surgery/adverse effects , Gastric Bypass/adverse effects , Obesity/complications , Obesity/diagnosis , Obesity/surgery , Gastrectomy/adverse effects
3.
Ann Diagn Pathol ; 60: 152014, 2022 Oct.
Article in English | MEDLINE | ID: mdl-35905536

ABSTRACT

Malignant rhabdoid tumor of the kidney (MRTK) is a rare aggressive pediatric renal tumor which can be diagnosed via fine-needle aspiration (FNA) cytology and core biopsy. The diagnosis of MRTK is challenging, and requires morphologic, immunohistochemical and clinical correlation to distinguish it from other entities. The differential diagnosis includes Wilms tumor, desmoplastic small round cell tumor, rhabdomyosarcoma, synovial sarcoma, renal medullary carcinoma, and epithelioid sarcoma. Here we describe a case of MRTK diagnosed on renal cytology and core biopsy with immunohistochemistry and follow by nephrectomy with gross and morphologic findings.


Subject(s)
Kidney Neoplasms , Rhabdoid Tumor , Biomarkers, Tumor , Child , Diagnosis, Differential , Humans , Immunohistochemistry , Kidney Neoplasms/diagnosis , Kidney Neoplasms/pathology , Rhabdoid Tumor/diagnosis , Rhabdoid Tumor/pathology , SMARCB1 Protein
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