18 July 2008
Osteosclerotic myeloma associated with spinal tuberculosis with neurological manifestation: A case report
Caroline Edijana Omoti, Ogbeide Ehimwenma, Osesogie Usualele OgbeideAm J Case Rep 2008; 9:321-324 :: ID: 864478
Abstract
Background: Coincidental presentation of osteosclerotic myeloma and spinal tuberculosis is an unusual and rare disease condition. Dissimilar data about diagnosis and treatment from various hospitals and different countries are reported. Spinal tuberculosis is the most dangerous form of tuberculous infection which commonly leads to a gradual onset of neurological defi cit that are difficult to diagnose at the early stage; and its association with osteosclerotic myeloma with multiorgan involvementincluding polyneuropathy, organomegaly, endocrinopathy, monoclonal gammopathy and skin changes, the so-called “POEMS” syndrome are rare.
Case Report: A 57-year-old male civil servant was admitted into the medical ward of the University of Benin Teaching Hospital (UBTH) Benin City, Nigeria on July 10th 2007 on account of one year history of cough, low backache and progressive weight loss. Examination showed grade 2 finger clubbing with leuconychia, sensory loss at T12, L1, and L4 with gibbus formation at T12, L1 which was nontender, bone marrow plasmacytosis (10%), serum protein electrophoresis showed a reduction of circulating IgG monoclonal protein; radiographs of the thoraco-lumbar spine revealed generalized osteosclerosis of the vertebrae and an anterior wedge fracture of T12, L1 and L4.
Conclusions: Coincidental presentation of osteosclerotic myeloma and spinal tuberculosis with neurological involvement is rare, but has been reported in this case occurring in an African. Effective management of these patients is multidisciplinary.
Keywords: osteosclerotic myeloma, spinal tuberculosis, neurological, peripheral neuropathy
In Press
Case report
Am J Case Rep In Press; DOI: 10.12659/AJCR.946151
Case report
Am J Case Rep In Press; DOI: 10.12659/AJCR.946630
Case report
Am J Case Rep In Press; DOI: 10.12659/AJCR.946954
Case report
Am J Case Rep In Press; DOI: 10.12659/AJCR.945924
Most Viewed Current Articles
21 Jun 2024 : Case report
93,646
DOI :10.12659/AJCR.944371
Am J Case Rep 2024; 25:e944371
07 Mar 2024 : Case report
51,228
DOI :10.12659/AJCR.943133
Am J Case Rep 2024; 25:e943133
20 Nov 2023 : Case report
28,109
DOI :10.12659/AJCR.941424
Am J Case Rep 2023; 24:e941424
18 Feb 2024 : Case report
23,005
DOI :10.12659/AJCR.943030
Am J Case Rep 2024; 25:e943030