Acute myocardial infarction treated with primary angioplasty in a rare form of hereditary thrombocytopenia: May-Hegglin anomaly. Clinical case and literature review;Infarto miocardico acuto trattato con angioplastica primaria in una rara forma di piastrinopenia ereditaria: Anomalia di May-Hegglin. Caso clinico e revisione della letteratura

Italian Heart Journal Supplement

Volumn 6, Issue 4, 2005, Pages 214-217

  Varbella, Ferdinando ^a   Bongioanni, Sergio ^a   Gagnor, Andrea ^a   Nannini, Cristiana ^a   La Brocca, Attilio ^b   Badalì, Antonio ^a   Conte, Maria Rosa ^a  

^a OSPEDALE DEGLI INFERMI   (Italy)

^b ASL 5   (Italy)

Author keywords

Coronary angioplasty; Myocardial infarction

Indexed keywords

ACUTE HEART INFARCTION; ADULT; ANGIOPLASTY; BALLOON DILATATION; CASE REPORT; FEMALE; FOLLOW UP; HOSPITALIZATION; HUMAN; MAY HEGGLIN ANOMALY; PERIPHERAL OCCLUSIVE ARTERY DISEASE; REVIEW; ST SEGMENT ELEVATION; THROMBOCYTOPENIA;

ANGIOPLASTY, TRANSLUMINAL, PERCUTANEOUS CORONARY; FEMALE; HUMANS; MIDDLE AGED; MYOCARDIAL INFARCTION; THROMBOCYTOPENIA;

EID: 29244471289     PISSN: 11294728     EISSN: None     Source Type: Journal    
DOI: None     Document Type: Review

References (15)

1. Martignetti JA, Heath KE, Harris J, et al. The gene for May-Hegglin anomaly localizes to a < 1-Mb region on chromosome 22q12.3-13.1. Am J Hum Genet 2000; 66: 1449-54.
2. Noris P, Spedini P, Belletti S, Magrini U, Balduini CL. Thrombocytopenia, giant platelets and leukocyte inclusion bodies (May-Hegglin anomaly): clinical and laboratory findings. Am J Med 1998; 104: 355-60.
3. Kunishima S. May-Hegglin anomaly - from genome research to clinical laboratory. Rinsho Byori 2003; 51: 898-904.
4. McDunn S, Hartz W Jr, Ts'Ao C, Green D. Coronary thrombosis in a patient with May-Hegglin anomaly. Am J Clin Pathol 1991; 95: 715-8.
5. Kelley MJ, Jawien W, Lin A, et al. Autosomal dominant macrothrombocytopenia with leukocyte inclusions (May-Hegglin anomaly) is linked to chromosome 22q12-12. Hum Genet 2000; 106: 557-64.
6. Jantunen E. Inherited giant platelet disorders. Eur J Haematol 1994; 53: 191-6.
7. Seri M, Cusano R, Gangrossa S, et al. Mutations in MYH9 result in May-Hegglin anomaly, and Fechtner and Sebastian syndromes. The May-Hegglin/Fechtner Syndrome Consortium. Nat Genet 2000; 26: 103-5.
8. Seri M, Pecci A, Di Bari F, et al. MYH9-related disease: May-Hegglin anomaly, Sebastian syndrome, Fechtner syndrome, and Epstein syndrome are not distinct entities but represent a variable expression of a single illness. Medicine 2003; 82: 203-15.
9. Everlien M, Knoch K, Farah I, Greve H. Coronary bypass surgery in May-Hegglin anomaly. Dtsch Med Wochenschr 2001; 126: 47-9.
10. Stouffer GA, Hirmerova J, Moll S, et al. Percutaneous coronary intervention in a patient with immune thrombocytopenia purpura. Catheter Cardiovasc Interv 2004; 61: 364-7.
11. Caputo RP, Abraham S, Churchill D. Transradial coronary stent placement in a patient with severe idiopathic autoimmune thrombocytopenic purpura. J Invasive Cardiol 2000; 12: 365-8.
12. Fuchi T, Kondo T, Sase K, Takahashi M. Primary percutaneous transluminal coronary angioplasty performed for acute myocardial infarction in a patient with idiopathic thrombocytopenic purpura. Jpn Circ J 1999; 63: 133-6.
13. Kikuchi S, Hayashi Y, Fujioka S, Kukita H, Ochi N. A case of intracoronary stent implanted for acute myocardial infarction in an elderly patient with idiopathic thrombocytopenic purpura. Nippon Ronen Igakkai Zasshi 2002; 39: 88-93.
14. Varbella F, Nannini C, Gagnor A, et al. Trattamento dell'infarto miocardico acuto con ST sopraslivellato mediante sistemi di tromboaspirazione ed angioplastica primaria. In: Atti del XXV Congresso Nazionale della Società Italiana di Cardiologia Invasiva. Napoli, 2004: 78.
15. Goodnough LT, Saito H, Ratnoff OD. Thrombosis or myocardial infarction in congenital clotting factor abnormalities and chronic thrombocytopenias: a report of 21 patients and a review of 50 previously reported cases. Medicine (Baltimore) 1983; 62: 248-55.