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https://www.readbyqxmd.com/read/27658328/a-case-of-hepatic-portal-venous-gas-after-colonoscopy
#1
Tevfik Solakoglu, Sevil O Sari, Huseyin Koseoglu, Murat Basaran, Mustafa Akar, Semnur Buyukasik, Osman Ersoy
Hepatic portal venous gas (HPVG) is a rare radiologic finding that is usually precipitated by intestinal ischaemia, intra-abdominal abscesses, necrotising enterocolitis, abdominal trauma, infectious enteritis, and inflammatory bowel disease. In this study, we present a case of HPVG in a 66-year-old female patient who underwent colonoscopy for evaluation of haematochezia and a review of the literature focused on HPVG following colonoscopy.
September 2016: Arab Journal of Gastroenterology: the Official Publication of the Pan-Arab Association of Gastroenterology
https://www.readbyqxmd.com/read/27559488/haematochezia-from-a-splenic-artery-pseudoaneurysm-communicating-with-transverse-colon-a-case-report-and-literature-review
#2
James O'Brien, Francesca Muscara, Aser Farghal, Irshad Shaikh
Splenic artery aneurysms (SAA) are the third most common intra-abdominal aneurysm. Complications include invasion into surrounding structures often in association with preexisting pancreatic disease. We describe an 88-year-old female, with no history of pancreatic disease, referred with lower gastrointestinal bleeding. CT angiography showed a splenic artery pseudoaneurysm with associated collection and fistula to the transverse colon at the level of the splenic flexure. The pseudoaneurysm was embolised endovascularly with metallic microcoils...
2016: Case Reports in Vascular Medicine
https://www.readbyqxmd.com/read/27107058/a-double-conundrum-concurrent-presentation-of-hashimoto-s-thyroiditis-and-ulcerative-colitis
#3
Gurpreet Singh, Susie Brien, Ellen Taylor
We describe a case of a 31-year-old man who presented with a 3-day history of crampy abdominal pain, anorexia, malaise and diarrhoea of increasing frequency, with the passage of both mucus and haematochezia. The patient's biochemical investigations revealed hyponatraemia, hypothyroidism and elevated inflammatory markers. The patient underwent an ultrasound and fine-needle aspiration of the thyroid and was diagnosed as having Hashimoto's thyroiditis. He was started on thyroxine and fluid was restricted. He was also investigated for alternative causes of hyponatraemia...
2016: BMJ Case Reports
https://www.readbyqxmd.com/read/27028211/clinical-presentation-treatment-and-outcome-in-31-dogs-with-presumed-primary-colorectal-lymphoma-2001-2013
#4
I Desmas, J H Burton, G Post, O Kristal, M Gauthier, J F Borrego, A Di Bella, A Lara-Garcia
The objective of this multicentre retrospective study was to describe clinical presentation, treatment and outcome and to determine prognostic factors for dogs with presumed primary colorectal lymphoma (PCRL). A total of 31 dogs were included. The predominant features of PCRL were high grade (n = 18) and immunophenotype B (n = 24). Most dogs were substage b (n = 25) with higher prevalence of haematochezia (n = 20). One dog had surgery only. Thirty dogs received chemotherapy; amongst them 13 had surgery or radiotherapy...
March 29, 2016: Veterinary and Comparative Oncology
https://www.readbyqxmd.com/read/26783491/gastrointestinal-bleeding-and-diffuse-skin-thickening-as-kaposi-sarcoma-clinical-presentation
#5
Sara Querido, Henrique Silva Sousa, Tiago Assis Pereira, Rita Birne, Patrícia Matias, Cristina Jorge, André Weigert, Teresa Adragão, Margarida Bruges, Domingos Machado
A 56-year-old African patient received a kidney from a deceased donor with 4 HLA mismatches in April 2013. He received immunosuppression with basiliximab, tacrolimus, mycophenolate mofetil, and prednisone. Immediate diuresis and a good allograft function were soon observed. Six months later, the serum creatinine level increased to 2.6 mg/dL. A renal allograft biopsy revealed interstitial fibrosis and tubular atrophy grade II. Toxicity of calcineurin inhibitor was assumed and, after a switch for everolimus, renal function improved...
2015: Case Reports in Transplantation
https://www.readbyqxmd.com/read/26712292/paediatric-endoscopy-by-adult-gastroenterologists-in-ile-ife-nigeria-a-viable-option-to-increase-the-access-to-paediatric-endoscopy-in-low-resource-countries
#6
Olusegun I Alatise, Henry Chineme Anyabolu, Oludayo Sowande, David Akinola
BACKGROUND: Paediatric endoscopy performed by adult gastroenterologists is a service delivery model that increases the access of children to endoscopy in countries where paediatric gastroenterologists with endoscopy skills are scarce. However, studies on the usefulness of this model in Nigeria and Sub-Saharan Africa are scarce. We aimed to evaluate the indications, procedures, diagnostic yield and safety of paediatric endoscopy performed by adult gastroenterologists in a Nigerian tertiary health facility...
October 2015: African Journal of Paediatric Surgery: AJPS
https://www.readbyqxmd.com/read/26548121/case-reports-of-adult-colo-colonic-intussusception
#7
O O Ayandipo, A I Abdurrazzaaq, G O Ogun, A T Adeniji-Sofoluwe, A F Ademola, T O Ogundiran
BACKGROUND: Adult colo-colonic intussusception is a rare abnormality and it may pose a diagnostic challenge. OBJECTIVE: To report two cases of adult colo-colonic intussusception with benign lesion as the lead points. METHODS: The Clinical records of the two patients containing the management details were retrieved and reviewed. RESULTS: The 1st case was a 60 year old man presenting with a year history of recurrent left abdominal pain a two week history of fullness left upper and lower abdomen...
March 2015: African Journal of Medicine and Medical Sciences
https://www.readbyqxmd.com/read/26430231/peutz-jeghers-syndrome-early-clinical-expression-of-a-new-stk11-gene-variant
#8
Sara Brito, Marta Póvoas, Juliette Dupont, Ana Isabel Lopes
Genetic heterogeneity has been recognised in Peutz-Jeghers syndrome (PJS) (over 230 STK11 gene mutations reported). We report a rare PJS phenotype with early extensive gastrointestinal (GI) presentation and a new genetic variant. The case presented as haematochezia and mucocutaneous pigmentation (the patient was 3 years of age). Endoscopy showed several polyps throughout the stomach/colon (PJ-type hamartomas); the larger polyps were resected. Small bowel imaging detected multiple jejunum/ileum small polyps...
2015: BMJ Case Reports
https://www.readbyqxmd.com/read/26313088/rectal-bleeding-and-endoscopy-need-in-sierra-leone-results-of-a-nationwide-community-based-survey
#9
Barclay T Stewart, Reinou S Groen, Thaim B Kamara, Steve Kwon, T Peter Kingham, Adam L Kushner
BACKGROUND: Low-income and middle-income countries (LMICs) face a large burden of gastrointestinal diseases that benefit from prompt endoscopic diagnosis and treatment. This study aimed to estimate the prevalence of gross rectal bleeding among adults in Sierra Leone. METHODS: A cluster randomised, cross-sectional household survey using the SOSAS tool was undertaken in Sierra Leone. 75 clusters of 25 households with two randomly selected respondents in each were sampled to estimate the prevalence of and disability from rectal bleeding...
April 27, 2015: Lancet
https://www.readbyqxmd.com/read/26242819/-heterotopic-gastric-mucosa-in-the-rectum-report-of-a-case
#10
Pablo Colsa-Gutiérrez, Mahgol Kharazmi-Taghavi, Rocío Daniela Sosa-Medina, José Ignacio Berrío-Obregón, Alfredo Ingelmo-Setién
BACKGROUND: Ectopic gastric mucosa has been described in different locations of the digestive tract, but that of the rectum is the least frequent. CLINICAL CASE: The case is described of a 48 year-old woman being investigated by the gastrointestinal department due to rectal bleeding and rectal tenesmus. Colonoscopy showed a diverticular cavity 3 cm, which was reported by histology as fundic-type heterotopic gastric mucosa. Barium enema and abdominopelvic CT showed a diverticular image at level of the right posterolateral wall of the rectal ampulla...
March 2016: Cirugia y Cirujanos
https://www.readbyqxmd.com/read/26004014/symptomatic-cytomegalovirus-gastrointestinal-infection-with-positive-quantitative-real-time-pcr-findings-in-apparently-immunocompetent-patients-a-case-series
#11
S Bernard, R Germi, J Lupo, M-H Laverrière, V Masse, P Morand, G Gavazzi
Cytomegalovirus (CMV) gastrointestinal disease rarely occurs in immunocompetent patients, and is mainly diagnosed on the basis of histopathological findings. Real-time PCR for CMV DNA quantification is considered to be a useful diagnostic tool, but its place in the diagnostic strategy is not clearly defined. The goal of the study was to describe the clinical and paraclinical features of apparently immunocompetent patients with CMV gastrointestinal disease diagnosed according to quantitative PCR results. In this retrospective study conducted in a 1500-bed tertiary-care centre, we reviewed the case records of apparently immunocompetent patients with positive findings of CMV DNA in gastrointestinal biopsies with compatible symptoms and endoscopic findings...
December 2015: Clinical Microbiology and Infection
https://www.readbyqxmd.com/read/25761296/-a-man-with-haematochezia-and-abdominal-pain
#12
Allard Aukema, Ellert J van Soest
A 83-year-old male was admitted to the Emergency Department with acute haematochezia and abdominal pain. At digital rectal examination multiple soft distensions were palpable. Sigmoidoscopy revealed ischaemia of the rectum with severe gangrene. The patient was discharged after fluid resuscitation. Follow-up sigmoidoscopy 4 weeks later showed a fully recovered rectum.
2015: Nederlands Tijdschrift Voor Geneeskunde
https://www.readbyqxmd.com/read/25684674/intestinal-lymphoid-nodular-hyperplasia-in-children-the-relationship-to-food-allergy
#13
RANDOMIZED CONTROLLED TRIAL
Sandra Lucarelli, Ginevra Lastrucci, Giovanni Di Nardo, Ylenia D'Alfonso, Marina Aloi, Salvatore Oliva, Simone Frediani, Danilo Rossetti, Tullio Frediani
BACKGROUND: Lymphoid nodular hyperplasia (LNH) of the lower gastrointestinal tract is a common finding during paediatric colonoscopies, and its clinical significance has not yet been clearly established. OBJECTIVE: The purpose of this prospective, parallel multi-arm, randomized clinical trial was to study relationship between food allergy and LNH. METHODS: We recruited 268 children who had undergone a diagnostic colonoscopy between 1 January 2009 and 30 September 2011...
February 2015: Pediatric Allergy and Immunology
https://www.readbyqxmd.com/read/25650379/a-28-year-old-woman-with-hypertrophic-right-leg-and-haematochezia
#14
Giuseppe Gizzi, Carlo Fabbri, Lorenzo Fuccio
No abstract text is available yet for this article.
October 2015: Gut
https://www.readbyqxmd.com/read/25492399/management-of-overt-upper-gastrointestinal-bleeding-in-a-low-resource-setting-a-real-world-report-from-nigeria
#15
Olusegun I Alatise, Adeniyi S Aderibigbe, Adewale O Adisa, Olusegun Adekanle, Augustine E Agbakwuru, Anthony O Arigbabu
BACKGROUND: Upper gastrointestinal bleeding (UGIB) remains a common medical problem worldwide that has significant associated morbidity, mortality, and health care resource use. This study outlines the aetiology, clinical presentation, and treatment outcomes of patients with UGIB in a Nigerian low resource health facility. METHODS: This was a descriptive study of consecutive patients who underwent upper gastrointestinal (GI) endoscopy for upper GI bleeding in the endoscopy unit of the Obafemi Awolowo University Teaching Hospital Complex, Ile-Ife, Osun State, Nigeria from January 2007 to December 2013...
2014: BMC Gastroenterology
https://www.readbyqxmd.com/read/25291873/giant-pedunculated-polypoid-submucosal-lipoma-of-the-splenic-flexure-of-colon-case-report-and-review-of-the-literature
#16
REVIEW
M R Zare-Khormizi, M Moghimi, F Pourrajab
Lipomas of the colon are rare but clinically important conditions that require suitable evaluation for guiding appropriate therapy. The majority of lipomas arise from the submucosal layer in the ascending colon, especially near the ileocecal valve, which causes difficulties in diagnosis. Giant lipomas may be misinterpreted as a premalignant adenomatous polyp, particularly when arising in the left colon. A 38-year-old man presented with manifestations including hypogastric pain, constipation, loss of appetite and weight, accompanied by anaemia, nausea, vomiting and haematochezia...
June 2014: Pathologica
https://www.readbyqxmd.com/read/25162963/symptomatic-paediatric-meckel-s-diverticulum-stratified-diagnostic-indicators-and-accuracy-of-meckel-s-scan
#17
Mazin Al Janabi, Madan Samuel, Andrea Kahlenberg, Sujith Kumar, Mina Al-Janabi
PURPOSE: The aim of the study was to delineate stratified diagnostic indicants and evaluate the diagnostic accuracy of technetium-99m (Tc)-pertechnetate scintigraphy in children with symptomatic Meckel's diverticulum (MD). MATERIALS AND METHODS: This was a prospective linear observational study conducted over a period of 5 years on 73 children with a diagnosis of symptomatic MD. The independent variables assessed were age, sex, weight-for-age z-scores, clinical presentation, complications of MD, laparoscopic findings, haematologic and biochemical results, radiological results, and histological findings...
November 2014: Nuclear Medicine Communications
https://www.readbyqxmd.com/read/25150239/rectal-ulcers-induced-by-systemic-lupus-erythematosus
#18
Alan Hoi Lun Yau, Karen Chu, Hui Min Yang, Hin Hin Ko
A 28-year-old woman presented with diarrhoea, haematochezia, tenesmus and rectal pain for 2 months. She was diagnosed with systemic lupus erythematosus (SLE) 8 years ago and remained on prednisone, azathioprine and hydroxychloroquine. Blood work revealed a positive ANA (antinuclear antibody test), anti-dsDNA 749 IU/mL (0-300 IU/mL), C3 0.22 g/L (0.65-1.65 g/L) and C4 0.05 g/L (0.16-0.60 g/L). Stool studies were unremarkable. MRI of the pelvis showed a rectum with eccentric wall thickening. Flexible sigmoidoscopy showed severe proctitis with multiple deep ulcers and diffuse submucosal haemorrhage...
2014: BMJ Case Reports
https://www.readbyqxmd.com/read/25141856/ethanol-sclerotherapy-of-rectal-venous-abnormalities-in-klippel-trenaunay-syndrome
#19
Nelson Agostinho, Ludi Ge, Michael J Solomon
Klippel-Trenaunay syndrome (KTS) is a rare congenital disorder characterized by the triad of capillary malformations, atypical venous malformations and varicosities and bony and/or soft tissue hypertrophy. We present the case of an 18-year-old man with KTS affected by haematochezia secondary to rectal venous malformations that was managed with endoscopic sclerotherapy. In this case, we compared the use of ethanol to phenol as a sclerosant.
2014: Journal of Surgical Case Reports
https://www.readbyqxmd.com/read/25097054/early-onset-of-dysplasia-in-polyps-in-children-with-familial-adenomatous-polyposis-case-report-and-literature-review
#20
REVIEW
Aleksandra Boskovic, Slavisa Djuricic, Blagoje Grujic, Ivica Stankovic
UNLABELLED: Familial adenomatous polyposis (FAP) is one of the most common hereditary syndromes associated with an increased risk of colorectal cancer. Onset of polyp formation and cancer in childhood is very unusual but has recently been associated with a specific mutation at codon 1309 in exon 15 where a more severe phenotype is sometimes observed .We report a 12-year-old girl who presented with haematochezia. The girl's mother and aunt had died of colon cancer which developed from untreated FAP...
June 2014: Arab Journal of Gastroenterology: the Official Publication of the Pan-Arab Association of Gastroenterology
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