Gene/Protein Disease Symptom Drug Enzyme Compound
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Query: UMLS:C0085693 (acute appendicitis)
 3,606 document(s) hit in 31,850,051 MEDLINE articles (0.00 seconds)

A 35-year-old patient with hemophilia A presented with rapidly progressive polyarteritis nodosa (PAN). He had been infected with hepatitis B virus (HBV) by repeated transfusion and was positive for hepatitis B surface antigen but negative for hepatitis B surface antibody. The patient presented symptoms of acute epididymitis followed by emergency admission because of acute appendicitis. On day 7 of admission, he complained of severe back pain, and computerized tomography (CT) showed massive perirenal hematoma. On day 49, mild monoplegia in the left arm suddenly developed, and CT and magnetic resonance imaging revealed multiple cerebral infarctions. Factor VIII replacement therapy was attenuated; however, cerebral infarction was progressive and extended throughout the cerebral hemispheres. He was diagnosed with classic polyarteritis nodosa (cPAN), and pulse methylprednisolone was continued. The patient died of supratentorial herniation, and autopsy revealed that vasculitis associated with intimal thickening was present in the liver, pancreas, intestine, kidneys, and larger-sized cerebral arteries. The development of cPAN appeared to have originated from chronic HBV infection, and this is the first report of cPAN in hemophilia patients. Concomitant hemorrhagic and thrombotic manifestations of cPAN are hardly treatable in patients with coagulation disorders, and the current case may represent a rare transfusion-related complication in hemophilia patients.
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PMID:Classic polyarteritis nodosa presenting rare clinical manifestations in a patient with hemophilia A. 1678 73

Primary appendiceal neoplasms are uncommon, being found in approximately 0.5%-1.0% of appendectomy specimens at pathologic evaluation. Primary appendiceal Burkitt's lymphomas are rare occurring in 0.015% of all gastrointestinal lymphomas. Almost all reported cases of appendiceal lymphoma have proved to be non-Hodgkin lymphoma. The majority of appendiceal lymphomas are of B-cell. Patients were almost entirely males. Acute appendicitis is the most common clinical manifestation. This report describes a rare case of primary appendiceal lymphoma in a patient presented with hematuria and dull aching right lower abdominal and back pain.
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PMID:Unusual presentation for primary appendiceal lymphoma: A case report. 2313 74

The differential diagnosis of anuria in emergency department (ED) is broad. Secondary to intraabdominal mass pressure or infections, symptoms of micturation difficulties or disuria accompanying to back pain may arise with the interruption of sacral nerve stimulation. Here, we report a patient who admitted to ED with back pain and anuria and diagnosed acute appendicitis (AA) after advanced investigation despite of not to have any abdominal pain. A 36-year-old man admitted to our ED with a 6-h history of back pain and urination difficulty. 750mL of clear urine output was observed after bladder catheterization. Abdominal computerized tomography with intravenous contrast was used and revealed acute appendicitis. The patient consulted with a general surgeon and hospitalized for operation. After the operation, back pain was disappeared, and spontaneous micturition was seen. This case not only represents an uncommon manifestation of AA, but also alerts us to the importance of anatomical considerations when interpreting disease extent with imaging. In the differential diagnosis of back pain and urination difficulty, the rare possibility of AA should be taken into account. Because the presence of unusual findings, such as those associated with the urinary tract or lumbosacral pathologies, may further obscure the diagnosis and delay appropriate therapy.
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PMID:Different manifestation of a familiar diagnosis: From anuria to acute appendicitis. 2951 Sep 13

Endometriosis of the appendix is a very rare entity and commonly affects females in childbearing age. Clinical presentation might be confusing varying from asymptomatic to acute abdominal pain and often mimicks acute appendicitis or chronic pelvic pain. Diagnosis is generally made after pathological examination as operative findings are usually non-specific. This condition poses a diagnostic challenge to radiologists and surgeons altogether and we therefore report a case of a middle aged female who presented with both right lower quadrant and right lower back pain. Recent literature is reviewed and radiological findings discussed.
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PMID:A rare case of right lower quadrant pain. 3150 92