ABSTRACT
We describe a 37-yr-old man who developed central pontine myelinolysis (CPM) after allogeneic hematopoietic stem cell transplantation (HSCT) for acute lymphoblastic leukemia. After HSCT, desquamation developed on the whole body accompanied by hyperbilirubinemia. The liver biopsy of the patient indicated graft-versus-host disease- related liver disease, and the dose of methylprednisolone was increased. Then, the patient developed altered mentality with eye ball deviation to the left, for which electroencephalogram and magnetic resonance imaging (MRI) scans were done. Brain MRI scan demonstrated the imaging findings consistent with central pontine myelinolysis and extrapontine myelinolysis. He did not have any hyponatremia episode during hospitalization prior to the MRI scan. To the best of our knowledge, presentation of CPM after allogeneic HSCT is extremely rare in cases where patients have not exhibited any episodes of significant hyponatremia. We report a rare case in which hepatic dysfunction due to graft-versus-host disease has a strong association with CPM after HSCT.
Subject(s)
Adult , Humans , Male , Biopsy , Brain/pathology , Electroencephalography , Graft vs Host Disease , Hematopoietic Stem Cell Transplantation/adverse effects , Hyperbilirubinemia/etiology , Liver/pathology , Magnetic Resonance Imaging , Myelinolysis, Central Pontine/complications , Precursor Cell Lymphoblastic Leukemia-Lymphoma/complications , Time Factors , Treatment OutcomeABSTRACT
A case of Central Pontine Myelinolysis and Extrapontine Myelinolysis presented with dystonia, Parkinsonism, and pathological crying that developed few days after gradual correction of hyponatremia. EEG slowing was evident before onset of symptoms, and disappeared with clinical improvement. Thalamic lesions alone produced these features. It dramatically responded to the Trihexyphenidyl therapy. Thus, basal ganglia involvement is not mandatory to produce this clinical picture; early onset of symptoms, resolution of EEG slowing and prompt response to anticholinergics may indicate better prognosis.
Subject(s)
Crying , Dystonia , Myelinolysis, Central Pontine/complications , Humans , Middle Aged , Myelinolysis, Central Pontine/drug therapy , Myelinolysis, Central Pontine/psychology , Parkinsonian Disorders , Myelinolysis, Central Pontine/drug therapy , Myelinolysis, Central Pontine/psychology , Parkinsonian Disorders , Trihexyphenidyl/therapeutic useABSTRACT
Central pontine myelinolysis is a demyelinating affection of central pons diagnosed on the basis of characteristic MRI finding in an appropriate clinical setting. The condition has been described as universally fatal; however, recent reports of recovery have been documented. We report a case of central pontine and extra pontine myelinolysis, which presented with parkinsonian features apart from bulbar symptoms and made a remarkable recovery. A short review of the literature follows.
Subject(s)
Brain/pathology , Humans , Magnetic Resonance Imaging , Male , Middle Aged , Myelinolysis, Central Pontine/complications , Parkinson Disease/drug therapy , Pons/pathology , Vomiting/etiologyABSTRACT
Tha case of a 55 year old man who presented with severe global headache 8 hours after having been drinking heavily, and who over a two hour period developed deep coma and flaccid paralysis of all four extremities is reported. A CT scan of the brain was normal; however, on Magnetic Resonance Imaging (MRI) extensive hyperintense areas in the brain stem, mainly in the pons, were easily identified. Based upon the clinical and MRI findings a diagnosis of Central Pontine Myelinolysis was made. Following several months of supportive therapy the patient partially recovered and was able to leave the hospital.