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1.
Case Rep Gastroenterol ; 1(1): 84-9, 2007 Sep 20.
Artículo en Inglés | MEDLINE | ID: mdl-21487551

RESUMEN

Hepatosplenic gamma/delta T-cell lymphoma is a rare neoplasm of mature gamma/delta T-cells with sinusoidal infiltration of spleen, liver, and bone marrow. Patients are predominantly adolescent and young adult males and usually present with marked hepatosplenomegaly. Pancytopenia is another common finding. Despite an initial response to treatment, patients have a median survival of one to two years. In this report, we document a case of alcoholic hepatitis and methadone withdrawal masquerading unsuspected, hepatosplenic gamma/delta T-cell lymphoma with unusual CD20 positivity.

2.
Am J Gastroenterol ; 94(8): 2304-6, 1999 Aug.
Artículo en Inglés | MEDLINE | ID: mdl-10445572

RESUMEN

We describe a case of a 25-yr-old woman with ulcerative colitis who developed marked thrombocytopenia during treatment and upon rechallenge with oral mesalamine. In contrast to its parent drug, sulfasalazine, which has often been reported to cause serious blood disorders, particularly agranulocytosis, mesalamine has rately been implicated as a cause of serious blood disorders. Although previous cases of hematological toxicity have been described in patients taking mesalamine, none of these patients were rechallenged in an effort to prove causality between 5-aminosalicyclic acid and the hematological abnormality as well as outrule the possible "autoimmune" contribution of inflammatory bowel disease to the hematological toxicity of these agents. This report demonstrates that mesalamine has the potential, like sulphasalazine, to cause marked thrombocytopenia in an idiosyncratic fashion. All patients receiving mesalamine therapy, either orally or topically should have regular, complete blood profiles.


Asunto(s)
Colitis Ulcerosa/tratamiento farmacológico , Mesalamina/efectos adversos , Trombocitopenia/inducido químicamente , Adulto , Colitis Ulcerosa/sangre , Diagnóstico Diferencial , Relación Dosis-Respuesta a Droga , Femenino , Humanos , Mesalamina/administración & dosificación , Recuento de Plaquetas , Trombocitopenia/sangre
3.
Surg Endosc ; 10(4): 418-21, 1996 Apr.
Artículo en Inglés | MEDLINE | ID: mdl-8661792

RESUMEN

BACKGROUND: Malignant degeneration of gastroduodenal polyps has been noted in patients with familial adenomatous polyposis. To evaluate this problem further, patients with familial adenomatous polyposis were contacted and offered upper gastrointestinal tract endoscopy. METHODS: A prospective endoscopic examination was performed in 42 patients. RESULTS: The median age of patients at endoscopy was 35 years. The duration of known familial adenomatous polyposis at the time of endoscopy was 8 years. Polyps were visualized in 21 patients (50%). Gastric polyps were seen in 14 patients (33%), duodenal polyps were seen in 11 patients (26%), and ampullary polyps were seen in 7 patients (17%). Nine patients (43%) had polyps in more than one site. Adenomatous change was noted in 73% of duodenal lesions and in only 14% of gastric polyps. Surgical intervention was required in four patients; one patient had an early ampullary carcinoma, and three patients had severe dysplasia involving the duodenum or ampulla. All four patients had undergone a previous screening examination, results of which were normal in three patients. Compared with other patients, these four patients were older (median age, 58 years; p = 0.02) and had a longer duration of disease (median duration, 25 years; p = 0.002). CONCLUSIONS: All patients with familial adenomatous polyposis require lifelong endoscopic surveillance to detect malignant degeneration, which may appear later in life.


Asunto(s)
Poliposis Adenomatosa del Colon/complicaciones , Neoplasias Duodenales/diagnóstico , Endoscopía del Sistema Digestivo , Pólipos/diagnóstico , Neoplasias Gástricas/diagnóstico , Adolescente , Adulto , Niño , Neoplasias Duodenales/complicaciones , Neoplasias Duodenales/epidemiología , Femenino , Estudios de Seguimiento , Humanos , Masculino , Persona de Mediana Edad , Pólipos/complicaciones , Prevalencia , Estudios Prospectivos , Factores de Riesgo , Neoplasias Gástricas/complicaciones , Neoplasias Gástricas/epidemiología
4.
J Clin Gastroenterol ; 19(4): 274-7, 1994 Dec.
Artículo en Inglés | MEDLINE | ID: mdl-7876504

RESUMEN

We have evaluated the diagnostic value of the fecal occult blood test (FOBT) in hospitalized patients. We reviewed the medical records of patients who had a positive FOBT not associated with a large gastrointestinal bleed, and who had a subsequent complete evaluation of their gastrointestinal (GI) tract. Of the 50 subjects who met the study criteria, 21 had various GI symptoms and 13 reported weight loss. Patients taking medications that may influence the FOBT result were distributed as follows: 15 were taking nonsteroidal antiinflammatory drugs, eight were taking iron supplementation, three were using steroid drugs, and three were taking anticoagulant drugs. Nonneoplastic lesions were found in 47 patients. Neoplastic lesions were discovered in 11 patients: seven had adenomatous polyps, two had colorectal cancer, one had gastric cancer, and one had duodenal cancer. Only two of seven patients with adenomatous polyps had lesions > 1 cm. In the study population, the positive predictive value of FOBT for finding colonic neoplasms was 18% and for any GI neoplasm it was 22%. Our data indicate that in hospitalized patients (a) the yield of colonic neoplasms from FOBT is approximately 50% less than that in healthy outpatients, and (b) a positive FOBT test is unlikely to lead to the detection of GI malignancy in the absence of suggestive clinical findings.


Asunto(s)
Neoplasias Gastrointestinales/diagnóstico , Hospitalización , Sangre Oculta , Adulto , Anciano , Anciano de 80 o más Años , Diagnóstico Diferencial , Femenino , Enfermedades Gastrointestinales/diagnóstico , Hemorragia Gastrointestinal/diagnóstico , Hemorragia Gastrointestinal/etiología , Humanos , Masculino , Persona de Mediana Edad , Valor Predictivo de las Pruebas , Estudios Retrospectivos
6.
Gastroenterology ; 101(6): 1756, 1991 Dec.
Artículo en Inglés | MEDLINE | ID: mdl-1955146
9.
N Engl J Med ; 322(23): 1674, 1990 06 07.
Artículo en Inglés | MEDLINE | ID: mdl-2342530
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