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Central Pontine Myelinosis and Osmotic Demyelination Syndrome

Journal

DEUTSCHES ARZTEBLATT INTERNATIONAL
Volume 116, Issue 35-36, Pages 600-+

Publisher

DEUTSCHER AERZTE-VERLAG GMBH
DOI: 10.3238/arztebl.2019.0600

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Background: Osmotic demyelination syndrome (ODS), which embraces central pontine myelinolysis (CPM) and extrapontine myelinosis (EPM), is often underdiagnosed in clinical practice, but can be fatal. In this article, we review the etiology, pathophysiology, clinical features, diagnosis. treatment, and prognosis of ODS. Methods: Pertinent publications from the years 1959 to 2018 were retrieved by a selective search in PubMed. Crystal structures of the three polymorphs of Cu-5(PO4)(2) (OH)(4) , namely pseudomalachite, ludjibaite, and reichenbachite, can be described as being composed of rods perpendicular to their crystal-chemical layering. Two different sorts of rods can be defined. Type 1 rods share rows of Cu coordination polyhedra, forming a series of pI slabs. Slab boundaries and slab interiors represent alternating geometric OD layers of two kinds, with layer symmetries close to P2(1)/m and P (1) over bar, which make up two different stacking schemes of geometric OD layers in the structures of ludjibaite and pseudomalachite. Such OD layers, however, are not developed in reichenbachite. Type 2 rods are defined as having columns of PO4 tetrahedra in the corners of the rods. In the Type 2 slabs composed of these rods, geometric Pg OD layers of glide-arrayed tetrahedra alternate with more complex P (1) over bar OD layers; in ludjibaite this system of layers is oriented diagonally with respect to the Type 1 OD layer system. Two different OD stockings of Type 2 OD layers form the ludjibaite and reichenbachite structures but not that of pseudomalachite. Thus, ludjibaite might form disordered intergrowths with either of the other two members of the triplet but reichenbachite and pseudomalachite should not firm oriented intergrowths. Current knowledge concerning formation of the three polymorphs is considered. Conclusion: ODS is a secondary neurological illness resulting from a foregoing primary disease. Though rare overall, it occurs with greater frequency in certain groups of patients. Clinicians of all specialties should therefore be familiar with the risk constellations, clinical presentation, and prevention of ODS. The treatment of ODS is still experimental at present, as no evidence-based treatment is yet available.

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