Gene/Protein Disease Symptom Drug Enzyme Compound
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Query: UMLS:C0033377 (prolapse)
 11,717 document(s) hit in 31,850,051 MEDLINE articles (0.00 seconds)

The purpose of our work is to study atrial depolarization in primary mitral prolapse (MVP), since, as far as we know, such a study has never been performed. Thirty patients with MVP were studied: 23 females, aged 37,3 +/- 15,5 years and 7 males, aged 45.1 +/- 18.1 years. MVP was diagnosed by M-mode echocardiography. Atrial depolarization was analysed on photographically recorded Frank's vectorcardiograms. On PsE loops, magnitude and direction of maximum planar vector (VMax) in the frontal (F) and left sagittal (LS) planes, magnitude and direction of anterior (HV1) and posterior (HV2) vectors in the horizontal (H) plane, HV1 to HV2 amplitude ratio and total atrial activation time (T) were measured. This last value (T), measured on vectorcardiographic records, was confirmed by high-speed (200 mm/sec) electrocardiograms. These data were compared, by mean of Student's test, with those measured on records obtained from a similar group of normals. The following statistically significant (P less than 0.05) differences were detected: decreased amplitude of VMax in F (0.11 +/- 0.03 vs. 0.080 +/- 0.03) and LS (0.11 +/- 0.03 vs. 0.085 +/- 0.03), backward shift of HV2 (+65 degrees +/- 39 degrees vs. + 11 degrees +/- 35 degrees) and decreased T (98 +/- 25 vs. 85 +/- 17). The decrease of total atrial activation time, about 13% less than in normals, is the most interesting finding of our research. Such an alteration of atrial depolarization can be explained by inter- and/or intra-atrial conduction disturbance, on anatomical or functional base. Therefore, our findings are consistent either with the hypothesis that MVP is secondary to widespread pathological changes or with the one that MVP is a consequence of neurovegetative imbalance.
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PMID:[Vectorcardiographic analysis of atrial activation in isolated mitral valve prolapse. Atrial vectorcardiography in prolapsed mitral valve]. 716 56

Hemolytic anemia is a well-recognized complication of mechanical heart valve prosthesis but, as yet, has not been reported after mitral valve repair with chordal replacement. We report a case of severe hemolytic anemia after mitral valve repair with chordal replacement and Carpentier-Edwards annuloplasty ring insertion. Progressive prolapse of the anterior leaflet due to the artificial chordae being too long caused recurrent regurgitation which was responsible for the hemolysis. The patient also had idiopathic thrombocytopenic purpura, but successful second mitral valve repair was performed after high-dose gamma-globulin therapy.
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PMID:Severe hemolysis due to artificial chordae displacement. 904 81

Pituitary apoplexy can occur as a complication of idiopathic thrombocytopenic purpura. We report here a new case of such association. A male patient aged 59 years, complaining of decreased libido for one year, was referred to the emergency department for purpura and severe thrombocytopenia (4000 platelets/mm3). 24 hours after the cutaneous rash the patient presented with clinical symptoms of bilateral cavernous sinus compression comprising ptosis, bilateral ophtalmoplegia and right supraorbital hypoesthesia. Cranial CT scan showed an enlarged sella and a pituitary mass with signs of intrapituitary haemorrhage. Hormonal evaluation showed hyperprolactinemia (50 ng/mL) and hypopituitarism, and the patient needed substitution with hydrocortisone and levothyroxine. Immunoglobulins and corticosteroids were given to the patient to treat thrombocytopenia, then worsening of neurological and ophtalmological symptoms led to pituitary surgery. Histopathological examination found necrotical pituitary tissue. Immunostaining with an anti-prolactin antibody was positive in several groups of cells. Neurological symptoms subsided and thrombocytopenia was corrected by treatment. In conclusion, we report a case of pituitary apoplexy due to severe thrombocytopenia occurring as a complication of a preexisting macroprolactinoma.
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PMID:Pituitary apoplexy and idiopathic thrombocytopenic purpura: a new case and review of the literature. 1632 68

Vincristine is a vinca alkaloid used in combination with other agents in the treatment of solid tumors, lymphoma, and leukemia, as well as for idiopathic thrombocytopenic purpura and autoimmune hemolytic anemia. A dose-limiting complication of vinca alkaloids is neurotoxicity. Vincristine is the oldest and also the most neurotoxic agent in this group. Described here is the case of a 4-year-old girl with unilateral palpebral ptosis. She has been diagnosed with precursor B-cell acute lymphoblastic leukemia. Ptosis was noted on the 45th day of therapy, and the last vincristine was administered on the 28th day of protocol 1. Vincristine-induced unilateral palpebral ptosis is a novel finding. Experience with this case suggests conservative treatment, with periodic examination, especially if ptosis is mild.
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PMID:Vincristine-induced unilateral ptosis in a child. 1993 Nov 72