Evidence map›Paper›PMID 38898638›Full record

ArticleThe American journal of case reports2024

A Rare Case of Hyperglycemia, Ketoacidosis, and Central Facial Paralysis in a Newly-Diagnosed Diabetic Woman.

Job Osango Omba, Robert Mutombo Kabasele, Nathan Tsengele, Cyprien Kavula, Antoine Salambo, John Bukasa Kakamba, Bertrand De Toffol

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In one paragraph

Article in The American journal of case reports, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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4 · The record

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5 · Who and what money

Authors and funding

7 authors.

Job Osango OmbaFaculty of Medicine, University of Kikwit, Kikwit, Congo, the Democratic Republic of the.ORCID 0009-0008-4897-1574
Robert Mutombo KabaseleDepartment of Neurology, Neuropsychopathologic Center, University of Kinshasa, Kinshasa, Congo, the Democratic Republic of the.
Nathan TsengeleFaculty of Medicine, University of Kikwit, Kikwit, Congo, the Democratic Republic of the.
Cyprien KavulaFaculty of Medicine, University of Kikwit, Kikwit, Congo, the Democratic Republic of the.
Antoine SalamboDepartment of Neurology, Neuropsychopathologic Center, University of Kinshasa, Kinshasa, Congo, the Democratic Republic of the.
John Bukasa KakambaDepartment of Endocrinology, CHU de Liège, Université de Liège, Liège, Belgium.
Bertrand De ToffolDepartment of Neurology, Cayenne Hospital Center, Cayenne, French Guiana.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

BACKGROUND Diabetes mellitus is a chronic disease that occurs when the pancreas does not produce enough insulin or when the body is unable to effectively use the insulin it produces. Uncontrolled diabetes mellitus is usually associated with neurological manifestations, such as hemichorea, focal epileptic seizures, peripheral neuropathy, and peripheral facial paralysis. This report describes a 59-year-old woman presenting with hyperglycemia and ketoacidosis due to newly diagnosed diabetes mellitus, as well as a temporary episode of central facial paralysis, which regressed within a few days after medical treatment and metabolic correction. CASE REPORT A 59-year-old patient with hypertension and a family history of diabetes mellitus presented with polyuro-polydipsic syndrome and signs of metabolic ketoacidosis, with an elevated anion gap, compatible with newly discovered type 1 diabetes mellitus. Six hours after admission, we noted the abrupt onset of left central facial paralysis, with no brain damage shown on magnetic resonance imaging. Initially, the diagnosis was transient ischemic attack. After a second, normal cerebral magnetic resonance image on the fourth day, and clinical improvement on the fifth day after metabolic correction by insulin therapy and rehydration, the diagnosis of a regressive central facial paralysis was retained. CONCLUSIONS Central facial paralysis in diabetic ketoacidosis is a rare neuroendocrine entity. The pathophysiological mechanisms that can explain the occurrence of central facial paralysis are not yet described and require further investigation. This report highlights the importance of diagnosis, early management of hyperglycemia and diabetic ketoacidosis, and reversibility of central facial paralysis after treatment.

Indexed as

Diabetes Mellitus, Type 1Diabetic KetoacidosisFacial ParalysisHyperglycemiaFemaleHumansHypoglycemic AgentsInsulinMiddle AgedHypoglycemic AgentsInsulin

Identifiers

PMID38898638
PMCPMC11334088

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.