Hermansky-Pudlak Syndrome: A Case Report

Objective. The aim of this paper is to report the case of a patient diagnosed with Hermansky-Pudlak syndrome, as a result of bleeding diathesis. Clinical Presentation and Intervention. A 23-year-old male presented with recurrent epistaxis and, upon physical examination, was found to be remarkable fo...

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Main Authors: Ilhami Berber, Mehmet Ali Erkurt, Irfan Kuku, Emin Kaya, Mustafa Koroglu, Ilknur Nizam, Mehmet Gul, Recep Bentli
Format: Article
Language:English
Published: Hindawi Limited 2014-01-01
Series:Case Reports in Hematology
Online Access:http://dx.doi.org/10.1155/2014/249195
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spelling doaj-5427c78ab6b246b5b761366248f144712020-11-25T01:08:16ZengHindawi LimitedCase Reports in Hematology2090-65602090-65792014-01-01201410.1155/2014/249195249195Hermansky-Pudlak Syndrome: A Case ReportIlhami Berber0Mehmet Ali Erkurt1Irfan Kuku2Emin Kaya3Mustafa Koroglu4Ilknur Nizam5Mehmet Gul6Recep Bentli7Department of Haematology, Faculty of Medicine, Inonu University, 44280 Malatya, TurkeyDepartment of Haematology, Faculty of Medicine, Inonu University, 44280 Malatya, TurkeyDepartment of Haematology, Faculty of Medicine, Inonu University, 44280 Malatya, TurkeyDepartment of Haematology, Faculty of Medicine, Inonu University, 44280 Malatya, TurkeyDepartment of Haematology, Faculty of Medicine, Inonu University, 44280 Malatya, TurkeyDepartment of Haematology, Faculty of Medicine, Inonu University, 44280 Malatya, TurkeyDepartment of Histology and Embryology, Faculty of Medicine, Inonu University, 44280 Malatya, TurkeyDepartment of Internal Medicine, Faculty of Medicine, Inonu University, 44280 Malatya, TurkeyObjective. The aim of this paper is to report the case of a patient diagnosed with Hermansky-Pudlak syndrome, as a result of bleeding diathesis. Clinical Presentation and Intervention. A 23-year-old male presented with recurrent epistaxis and, upon physical examination, was found to be remarkable for albinism and suborbital ecchymosis. The absence of dense bodies in the platelets was demonstrated using electron microscopy. This patient was (slowly) administered one unit of a platelet suspension, and his bleeding decreased considerably. Conclusion. This case shows that Hermansky-Pudlak syndrome should be considered in the differential diagnosis of a patient presenting with bleeding diathesis, when the clinical presentation also includes oculocutaneous albinism and visual problems.http://dx.doi.org/10.1155/2014/249195
collection DOAJ
language English
format Article
sources DOAJ
author Ilhami Berber
Mehmet Ali Erkurt
Irfan Kuku
Emin Kaya
Mustafa Koroglu
Ilknur Nizam
Mehmet Gul
Recep Bentli
spellingShingle Ilhami Berber
Mehmet Ali Erkurt
Irfan Kuku
Emin Kaya
Mustafa Koroglu
Ilknur Nizam
Mehmet Gul
Recep Bentli
Hermansky-Pudlak Syndrome: A Case Report
Case Reports in Hematology
author_facet Ilhami Berber
Mehmet Ali Erkurt
Irfan Kuku
Emin Kaya
Mustafa Koroglu
Ilknur Nizam
Mehmet Gul
Recep Bentli
author_sort Ilhami Berber
title Hermansky-Pudlak Syndrome: A Case Report
title_short Hermansky-Pudlak Syndrome: A Case Report
title_full Hermansky-Pudlak Syndrome: A Case Report
title_fullStr Hermansky-Pudlak Syndrome: A Case Report
title_full_unstemmed Hermansky-Pudlak Syndrome: A Case Report
title_sort hermansky-pudlak syndrome: a case report
publisher Hindawi Limited
series Case Reports in Hematology
issn 2090-6560
2090-6579
publishDate 2014-01-01
description Objective. The aim of this paper is to report the case of a patient diagnosed with Hermansky-Pudlak syndrome, as a result of bleeding diathesis. Clinical Presentation and Intervention. A 23-year-old male presented with recurrent epistaxis and, upon physical examination, was found to be remarkable for albinism and suborbital ecchymosis. The absence of dense bodies in the platelets was demonstrated using electron microscopy. This patient was (slowly) administered one unit of a platelet suspension, and his bleeding decreased considerably. Conclusion. This case shows that Hermansky-Pudlak syndrome should be considered in the differential diagnosis of a patient presenting with bleeding diathesis, when the clinical presentation also includes oculocutaneous albinism and visual problems.
url http://dx.doi.org/10.1155/2014/249195
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