Egy amegakaryocytás thrombocytás purpurához társult zománcfejlödési rendellenesség esete.

Translated title of the contribution: Megakaryocytic thrombopenic purpura associated with enamel hypoplasia

M. Alberth, J. Nemes, T. Radics, C. Kiss

Research output: Contribution to journalArticle

Abstract

Patients with platelet disorders usually bleed into superficial sites such as the skin, mucous membranes, genitourinary tract and gastrointestinal tract caused by thrombocytopenia or thrombocyte dysfunction. Thrombocytopenia is caused by one of three mechanisms-decreased marrow production, increased splenic sequestration, or accelerated destruction of platelets. We report a 9-year-old male patient with thrombocytopenic purpura, dyserythropoetic anaemia, freckles on the skin and nanosomia, resembling Fanconi's (constitutional) anaemia. Although many patients with constitutional anaemia own other bony abnormalities, it was not found in this case. On the other hand, the patient showed enamel hypoplasia. To our knowledge, this association has never been reported before. Laboratory diagnosis, clinical findings, dental abnormalities and treatment are presented in details.

Original languageHungarian
Pages (from-to)131-135
Number of pages5
JournalFogorvosi szemle
Volume90
Issue number5
Publication statusPublished - 1997

Fingerprint

Dental Enamel Hypoplasia
Thrombocytopenic Purpura
Blood Platelets
Thrombocytopenia
Anemia
Tooth Abnormalities
Fanconi Anemia
Melanosis
Skin
Clinical Laboratory Techniques
Gastrointestinal Tract
Mucous Membrane
Bone Marrow

Cite this

Egy amegakaryocytás thrombocytás purpurához társult zománcfejlödési rendellenesség esete. / Alberth, M.; Nemes, J.; Radics, T.; Kiss, C.

In: Fogorvosi szemle, Vol. 90, No. 5, 1997, p. 131-135.

Research output: Contribution to journalArticle

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abstract = "Patients with platelet disorders usually bleed into superficial sites such as the skin, mucous membranes, genitourinary tract and gastrointestinal tract caused by thrombocytopenia or thrombocyte dysfunction. Thrombocytopenia is caused by one of three mechanisms-decreased marrow production, increased splenic sequestration, or accelerated destruction of platelets. We report a 9-year-old male patient with thrombocytopenic purpura, dyserythropoetic anaemia, freckles on the skin and nanosomia, resembling Fanconi's (constitutional) anaemia. Although many patients with constitutional anaemia own other bony abnormalities, it was not found in this case. On the other hand, the patient showed enamel hypoplasia. To our knowledge, this association has never been reported before. Laboratory diagnosis, clinical findings, dental abnormalities and treatment are presented in details.",
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