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Brentuximab vedotin-associated diabetic ketoacidosis: a case report

BACKGROUND: Diabetic ketoacidosis (DKA) is a life-threatening complication of diabetes mellitus (DM). It is characterized by hyperglycemia, metabolic acidosis, and ketonemia. Fortunately, drug-induced hyperglycemias are usually mild and not life-threatening. However, rarely some cases may present wi...

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Autores principales: Köksalan, Damla, Sözen, Mehmet, Selek, Alev, Gezer, Emre, Cantürk, Zeynep, Çetinarslan, Berrin
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Springer India 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9287688/
https://www.ncbi.nlm.nih.gov/pubmed/35875342
http://dx.doi.org/10.1007/s13410-022-01116-w
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author Köksalan, Damla
Sözen, Mehmet
Selek, Alev
Gezer, Emre
Cantürk, Zeynep
Çetinarslan, Berrin
author_facet Köksalan, Damla
Sözen, Mehmet
Selek, Alev
Gezer, Emre
Cantürk, Zeynep
Çetinarslan, Berrin
author_sort Köksalan, Damla
collection PubMed
description BACKGROUND: Diabetic ketoacidosis (DKA) is a life-threatening complication of diabetes mellitus (DM). It is characterized by hyperglycemia, metabolic acidosis, and ketonemia. Fortunately, drug-induced hyperglycemias are usually mild and not life-threatening. However, rarely some cases may present with ketoacidosis. In this case report, we aimed to present a brentuximab vedotin (BV) associated with DKA. CASE PRESENTATION: A 23-year-old Caucasian man presented with abdominal pain, nausea, and vomiting for 1–2 weeks. The patient had a previous diagnosis of Hodgkin’s lymphoma and primer hypothyroidism. He is using levothyroxine 150 μg per day and received BV treatment for Hodgkin lymphoma (HL) 10 days ago. No steroid treatment was administered for premedication before BV. Except for obesity, all system examinations are normal. There were no signs of any infection. Laboratory data revealed hyperglycemia, metabolic acidosis, and ketonemia. The patient was admitted to the service with a diagnosis of DKA. After the patient was admitted to our clinic, insulin treatment and hydration started immediately. Despite the insulin infusion reaching 1700 units per day, the patient’s diabetic ketoacidosis extended to 1 week. Anti-insulin, anti-glutamic acid decarboxylase, and islet cell autoantibodies were negative, which were checked to exclude type 1 DM. Fasting C-peptide was 28 ng/mL (normal range, 0.9–7.1 ng/mL). With all these, the diabetic ketoacidosis status of the patient was evaluated as a BV side effect. CONCLUSION: This patient is a rare case of BV-associated DKA. It is very important to know this relationship since BV treatment has turned into a standard treatment for relapsed Hodgkin lymphoma. Our case highlights that this diagnosis should be kept in mind as a complication of each dose of BV administration.
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spelling pubmed-92876882022-07-18 Brentuximab vedotin-associated diabetic ketoacidosis: a case report Köksalan, Damla Sözen, Mehmet Selek, Alev Gezer, Emre Cantürk, Zeynep Çetinarslan, Berrin Int J Diabetes Dev Ctries Case Report BACKGROUND: Diabetic ketoacidosis (DKA) is a life-threatening complication of diabetes mellitus (DM). It is characterized by hyperglycemia, metabolic acidosis, and ketonemia. Fortunately, drug-induced hyperglycemias are usually mild and not life-threatening. However, rarely some cases may present with ketoacidosis. In this case report, we aimed to present a brentuximab vedotin (BV) associated with DKA. CASE PRESENTATION: A 23-year-old Caucasian man presented with abdominal pain, nausea, and vomiting for 1–2 weeks. The patient had a previous diagnosis of Hodgkin’s lymphoma and primer hypothyroidism. He is using levothyroxine 150 μg per day and received BV treatment for Hodgkin lymphoma (HL) 10 days ago. No steroid treatment was administered for premedication before BV. Except for obesity, all system examinations are normal. There were no signs of any infection. Laboratory data revealed hyperglycemia, metabolic acidosis, and ketonemia. The patient was admitted to the service with a diagnosis of DKA. After the patient was admitted to our clinic, insulin treatment and hydration started immediately. Despite the insulin infusion reaching 1700 units per day, the patient’s diabetic ketoacidosis extended to 1 week. Anti-insulin, anti-glutamic acid decarboxylase, and islet cell autoantibodies were negative, which were checked to exclude type 1 DM. Fasting C-peptide was 28 ng/mL (normal range, 0.9–7.1 ng/mL). With all these, the diabetic ketoacidosis status of the patient was evaluated as a BV side effect. CONCLUSION: This patient is a rare case of BV-associated DKA. It is very important to know this relationship since BV treatment has turned into a standard treatment for relapsed Hodgkin lymphoma. Our case highlights that this diagnosis should be kept in mind as a complication of each dose of BV administration. Springer India 2022-07-16 2023-02 /pmc/articles/PMC9287688/ /pubmed/35875342 http://dx.doi.org/10.1007/s13410-022-01116-w Text en © The Author(s), under exclusive licence to Research Society for Study of Diabetes in India 2022 This article is made available via the PMC Open Access Subset for unrestricted research re-use and secondary analysis in any form or by any means with acknowledgement of the original source. These permissions are granted for the duration of the World Health Organization (WHO) declaration of COVID-19 as a global pandemic.
spellingShingle Case Report
Köksalan, Damla
Sözen, Mehmet
Selek, Alev
Gezer, Emre
Cantürk, Zeynep
Çetinarslan, Berrin
Brentuximab vedotin-associated diabetic ketoacidosis: a case report
title Brentuximab vedotin-associated diabetic ketoacidosis: a case report
title_full Brentuximab vedotin-associated diabetic ketoacidosis: a case report
title_fullStr Brentuximab vedotin-associated diabetic ketoacidosis: a case report
title_full_unstemmed Brentuximab vedotin-associated diabetic ketoacidosis: a case report
title_short Brentuximab vedotin-associated diabetic ketoacidosis: a case report
title_sort brentuximab vedotin-associated diabetic ketoacidosis: a case report
topic Case Report
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9287688/
https://www.ncbi.nlm.nih.gov/pubmed/35875342
http://dx.doi.org/10.1007/s13410-022-01116-w
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