Thromb Haemost 1981; 46(04): 722-724
DOI: 10.1055/s-0038-1653461
Original Article
Schattauer GmbH Stuttgart

Essential Athrombia

A Report of 4 Cases from South India
U Khanduri
The Department of Clinical Pathology and Blood Bank, Christian Medical College Hospital, Vellore, Tamil Nadu, India
,
R Pulimood
The Department of Clinical Pathology and Blood Bank, Christian Medical College Hospital, Vellore, Tamil Nadu, India
,
A Sudarasanam
The Department of Clinical Pathology and Blood Bank, Christian Medical College Hospital, Vellore, Tamil Nadu, India
,
R H Carman
The Department of Clinical Pathology and Blood Bank, Christian Medical College Hospital, Vellore, Tamil Nadu, India
,
M Jadhav
*   The Dept. of Child Health, Christian Medical College Hospital, Vellore, Tamil Nadu, India
,
S Pereira
*   The Dept. of Child Health, Christian Medical College Hospital, Vellore, Tamil Nadu, India
,
B M Pulimood
**   The Dept. of Medicine, Christian Medical College Hospital, Vellore, Tamil Nadu, India
› Author Affiliations
Further Information

Publication History

Received 10 March 1981

Accepted 01 October 1981

Publication Date:
05 July 2018 (online)

Summary

Four cases of essential athrombia have been diagnosed in the 14 year period from June, 1966 to June, 1980 at the Coagulation Laboratory of the Christian Medical College Hospital, Vellore. All cases fit Inceman’s description of the original case and fulfill the diagnostic criteria of prolonged bleeding time, decreased platelet aggregation, normal platelet count, normal morphology and normal clot retraction. No cases have been reported from India in the past 15 years.

 
  • References

  • 1 Inceman S. Thrombopathie hémorragique avec altération élective des fonctions d’agglutination. 1956. 5th Int Cong Haemat; Paris:
  • 2 Inceman S, Unügur A, Aran M. Essential Athrombia. Thrombos Diathes Haemorrh 1962; 8: 502-510
  • 3 Ulutin ON, Ulutin SB. Congenital Athrombias. Med Bull Istanbul 1970; 1971; 3-4: 81-91
  • 4 Ulutin ON. Qualitative platelet disorders–classification and pathogenesis. Ann NY Acad Sei 1972; 201: 176-193
  • 5 Dacie JV, Lewis SM. Practical Haematology. 1975. Churchill Livingstone: ELBS V edition;
  • 6 Hardisty RM, Hutton RA. Kaolin clotting time of platelet rich plasma – a test of platelet factor 3 availability. Br J Haematol 1965; 11: 258-268
  • 7 Borchgrevink CF. Platelet adhesion in vivo in patients with bleeding disorders. Acta Med Scand 1961; 170: 231-263
  • 8 Wooton DP. Micro analysis in Medical Biochemistry, 1974 V edition Churchill Livingstone. Assay of fibrinogen by turbidimetric method 158-159
  • 9 Goldman BA, Aledort LA. Essential athrombia–a family study. Ann Intern Med 1972; 76: 267-273
  • 10 Sundar Rao PS S, Inbaraj SG, Kaliaperumal VG. An epidemiological study of consanguinity in a large South Indian town. Indian J Med Res 1971; 59: 294-301
  • 11 Roychoudhury AK. Incidence of inbreeding in different states of India. Demography India 1975; 5: 108-119
  • 12 Khanduri U, Pulimood R, Sudarsanam A, Carman RH, Jadhav M, Pereira S. Glanzmann’s Thrombasthenia. A review and report of 42 cases from South India Thromb Haemostas 1981; 46: 717
  • 13 Hardisty RM, Hutton RA. Bleeding tendency associated with new abnormality of platelet behaviour. Lancet 1967; 1: 983-985
  • 14 Hirsh J, Castelan DJ, Loder PB. Spontaneous bruising associated with a defect in the interaction of platelets with connective tissue. Lancet 1967; 2: 18-21
  • 15 Sahud MA, Aggeler PM. Platelet dysfunction–differentiation of a newly recognised primary type from that produced by aspirin. N Engl J Med 1969; 28: 453-459
  • 16 Papayannis AG, Wood JK, Israels MC G. A new abnormality of platelet function. Acta Haematol 1970; 44: 98-110
  • 17 O’Brien JR. Platelets: a Portsmouth Syndrome?. Lancet 1967; 2: 258