Cargando…
Severe thrombocytosis and anemia associated with celiac disease in a young female patient: a case report
INTRODUCTION: Platelet counts exceeding 1.000 × 10(3)/μl are usually considered secondary to another cause, particularly to chronic myeloproliferative disease (CMPD). Reactive thrombocytosis due to iron deficiency rarely exceeds platelet counts of 700 × 10(3)/μl. CASE PRESENTATION: Here we report th...
Autores principales: | , , , , , |
---|---|
Formato: | Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2008
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2329657/ https://www.ncbi.nlm.nih.gov/pubmed/18380894 http://dx.doi.org/10.1186/1752-1947-2-96 |
_version_ | 1782152756254998528 |
---|---|
author | Voigt, Wieland Jordan, Karin Sippel, Christoph Amoury, Mroawan Schmoll, Hans-Joachim Wolf, Hans H |
author_facet | Voigt, Wieland Jordan, Karin Sippel, Christoph Amoury, Mroawan Schmoll, Hans-Joachim Wolf, Hans H |
author_sort | Voigt, Wieland |
collection | PubMed |
description | INTRODUCTION: Platelet counts exceeding 1.000 × 10(3)/μl are usually considered secondary to another cause, particularly to chronic myeloproliferative disease (CMPD). Reactive thrombocytosis due to iron deficiency rarely exceeds platelet counts of 700 × 10(3)/μl. CASE PRESENTATION: Here we report the case of a young woman presenting with clinical signs of severe anemia. Laboratory findings confirmed an iron-deficiency anemia associated with severe thrombocytosis of 1703 × 10(3)/μl. Macroscopic gastrointestinal and genitourinary tract bleeding was excluded. The excessive elevation of platelets, slightly elevated lactate dehydrogenase and slightly elevated leukocytes along with the absence of other inflammation parameters raised the suspicion of an underlying hematological disease. However, bone marrow evaluation could not prove the suspected diagnosis of a CMPD, especially essential thrombocythemia (ET). In the further clinical course the platelet count returned to normal after raising the hemoglobin to a level close to normal range with erythrocyte transfusion, and normalization of serum iron and decline of erythropoietin. Finally, following small bowel biopsy, despite the absence of typical clinical signs, celiac disease was diagnosed. After discharge from hospital the patient was commenced on a gluten-free diet and her hemoglobin almost completely normalized in the further follow-up period. CONCLUSION: This case illustrates the rare constellation of an extreme thrombocytosis most likely secondary to iron deficiency due to celiac disease. This represents, to the best of the authors' knowledge, the highest reported platelet count coincident with iron deficiency. A potential mechanism for the association of iron-deficiency anemia and thrombocytosis is discussed. Even in the presence of 'atypically' high platelets one should consider the possibility of reactive thrombocytosis. Extreme thrombocytosis could emerge in the case of iron deficiency secondary to celiac disease. |
format | Text |
id | pubmed-2329657 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2008 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-23296572008-04-23 Severe thrombocytosis and anemia associated with celiac disease in a young female patient: a case report Voigt, Wieland Jordan, Karin Sippel, Christoph Amoury, Mroawan Schmoll, Hans-Joachim Wolf, Hans H J Med Case Reports Case Report INTRODUCTION: Platelet counts exceeding 1.000 × 10(3)/μl are usually considered secondary to another cause, particularly to chronic myeloproliferative disease (CMPD). Reactive thrombocytosis due to iron deficiency rarely exceeds platelet counts of 700 × 10(3)/μl. CASE PRESENTATION: Here we report the case of a young woman presenting with clinical signs of severe anemia. Laboratory findings confirmed an iron-deficiency anemia associated with severe thrombocytosis of 1703 × 10(3)/μl. Macroscopic gastrointestinal and genitourinary tract bleeding was excluded. The excessive elevation of platelets, slightly elevated lactate dehydrogenase and slightly elevated leukocytes along with the absence of other inflammation parameters raised the suspicion of an underlying hematological disease. However, bone marrow evaluation could not prove the suspected diagnosis of a CMPD, especially essential thrombocythemia (ET). In the further clinical course the platelet count returned to normal after raising the hemoglobin to a level close to normal range with erythrocyte transfusion, and normalization of serum iron and decline of erythropoietin. Finally, following small bowel biopsy, despite the absence of typical clinical signs, celiac disease was diagnosed. After discharge from hospital the patient was commenced on a gluten-free diet and her hemoglobin almost completely normalized in the further follow-up period. CONCLUSION: This case illustrates the rare constellation of an extreme thrombocytosis most likely secondary to iron deficiency due to celiac disease. This represents, to the best of the authors' knowledge, the highest reported platelet count coincident with iron deficiency. A potential mechanism for the association of iron-deficiency anemia and thrombocytosis is discussed. Even in the presence of 'atypically' high platelets one should consider the possibility of reactive thrombocytosis. Extreme thrombocytosis could emerge in the case of iron deficiency secondary to celiac disease. BioMed Central 2008-04-01 /pmc/articles/PMC2329657/ /pubmed/18380894 http://dx.doi.org/10.1186/1752-1947-2-96 Text en Copyright © 2008 Voigt et al; licensee BioMed Central Ltd. http://creativecommons.org/licenses/by/2.0 This is an Open Access article distributed under the terms of the Creative Commons Attribution License ( (http://creativecommons.org/licenses/by/2.0) ), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Case Report Voigt, Wieland Jordan, Karin Sippel, Christoph Amoury, Mroawan Schmoll, Hans-Joachim Wolf, Hans H Severe thrombocytosis and anemia associated with celiac disease in a young female patient: a case report |
title | Severe thrombocytosis and anemia associated with celiac disease in a young female patient: a case report |
title_full | Severe thrombocytosis and anemia associated with celiac disease in a young female patient: a case report |
title_fullStr | Severe thrombocytosis and anemia associated with celiac disease in a young female patient: a case report |
title_full_unstemmed | Severe thrombocytosis and anemia associated with celiac disease in a young female patient: a case report |
title_short | Severe thrombocytosis and anemia associated with celiac disease in a young female patient: a case report |
title_sort | severe thrombocytosis and anemia associated with celiac disease in a young female patient: a case report |
topic | Case Report |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2329657/ https://www.ncbi.nlm.nih.gov/pubmed/18380894 http://dx.doi.org/10.1186/1752-1947-2-96 |
work_keys_str_mv | AT voigtwieland severethrombocytosisandanemiaassociatedwithceliacdiseaseinayoungfemalepatientacasereport AT jordankarin severethrombocytosisandanemiaassociatedwithceliacdiseaseinayoungfemalepatientacasereport AT sippelchristoph severethrombocytosisandanemiaassociatedwithceliacdiseaseinayoungfemalepatientacasereport AT amourymroawan severethrombocytosisandanemiaassociatedwithceliacdiseaseinayoungfemalepatientacasereport AT schmollhansjoachim severethrombocytosisandanemiaassociatedwithceliacdiseaseinayoungfemalepatientacasereport AT wolfhansh severethrombocytosisandanemiaassociatedwithceliacdiseaseinayoungfemalepatientacasereport |