Severe cobalamin deficiency disguised as schistocytes: A case report

dc.contributor.authorKoubaissi, Salwa A.
dc.contributor.authorDegheili, Jad A.
dc.contributor.departmentInternal Medicine
dc.contributor.departmentSurgery
dc.contributor.facultyFaculty of Medicine (FM)
dc.contributor.institutionAmerican University of Beirut
dc.date.accessioned2025-01-24T11:55:19Z
dc.date.available2025-01-24T11:55:19Z
dc.date.issued2019
dc.description.abstractChallenging differential diagnosis Vitamin B12, also known as cobalamin (Cbl), is a major player in both erythropoiesis and myelination of the central nervous system. The 2 main manifestations of vitamin B12 deficiency are bone marrow failure and demyelinating disease. These manifestations also depend on the severity and duration of the deficiency. In severe cases, ineffective erythropoiesis, with intramedullary destruction of erythrocytes has been reported, and increased homocysteine level was shown to be a cause of this hemolysis, in vitro. We present the case of a middle-aged man presented with worsening fatigue, pallor, and dyspnea on moderate exertion. He was found to have a macrocytic anemia associated with intravascular hemolysis and clinical hypothyroidism in the setting of Hashimoto’s thyroiditis. Vitamin B12 measured as part of his anemia investigation, was found to be markedly deficient (less than 100 pg/mL). Replacement was started and a reversal of his anemia and hemolysis was shown with improvement in his hemoglobin level upon follow-up. Although a rare presentation, severe vitamin B12 deficiency can lead to hemolysis and severe anemia that can be life threatening. Timely and appropriate diagnosis and replacement, lifelong in some cases, in addition to looking for the underlying cause of this deficiency, and excluding other concomitant hemolytic disorders, is crucial for the management of this reversible disease. Despite some in vitro early results, the exact underlying mechanism behind hemolysis is still unclear. © Am J Case Rep,2019.
dc.identifier.doihttps://doi.org/10.12659/AJCR.918807
dc.identifier.eid2-s2.0-85075114466
dc.identifier.pmid31734686
dc.identifier.urihttp://hdl.handle.net/10938/31199
dc.language.isoen
dc.publisherInternational Scientific Information, Inc.
dc.relation.ispartofAmerican Journal of Case Reports
dc.sourceScopus
dc.subjectAnemia
dc.subjectHemolytic
dc.subjectHomocysteine
dc.subjectPernicious
dc.subjectVitamin b 12 deficiency
dc.subjectAnemia, hemolytic
dc.subjectDiagnosis, differential
dc.subjectErythrocyte transfusion
dc.subjectHashimoto disease
dc.subjectHumans
dc.subjectMale
dc.subjectMiddle aged
dc.subjectThyroxine
dc.subjectVitamin b 12
dc.subjectCyanocobalamin
dc.subjectHemoglobin
dc.subjectLevothyroxine
dc.subjectAdult
dc.subjectArthralgia
dc.subjectArticle
dc.subjectBlood transfusion
dc.subjectBody weight disorder
dc.subjectCase report
dc.subjectCaucasian
dc.subjectClinical article
dc.subjectClinical examination
dc.subjectComorbidity
dc.subjectCoronary artery disease
dc.subjectDiet therapy
dc.subjectDisease association
dc.subjectDisease severity
dc.subjectDizziness
dc.subjectDyspnea
dc.subjectErythrocyte culture
dc.subjectErythrocyte disorder
dc.subjectFamily history
dc.subjectFather-in-law
dc.subjectFatigue
dc.subjectHemoglobin blood level
dc.subjectHemolytic uremic syndrome
dc.subjectHuman
dc.subjectHuman cell
dc.subjectHypothyroidism
dc.subjectIntravascular hemolysis
dc.subjectLaboratory test
dc.subjectMacrocytic anemia
dc.subjectNon-smoker
dc.subjectPallor
dc.subjectPernicious anemia
dc.subjectSchistocyte
dc.subjectSclera disease
dc.subjectThrombotic thrombocytopenic purpura
dc.subjectTransluminal coronary angioplasty
dc.subjectUpper respiratory tract infection
dc.subjectComplication
dc.subjectCyanocobalamin deficiency
dc.subjectDifferential diagnosis
dc.subjectHemolytic anemia
dc.titleSevere cobalamin deficiency disguised as schistocytes: A case report
dc.typeArticle

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