Neuropathic arthropathy of the shoulder joint secondary to a syringomyelia.
Neuropathic arthropathy of the shoulder joint secondary to a syringomyelia.
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DOI:
10.1136/bcr-2018-228228
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发表时间:
2018-12-03
期刊:
影响因子:
0.9
通讯作者:
Pai, Vishal
中科院分区:
文献类型:
--
作者:
Nambiar, Mithun;Onggo, James Randolph;Pai, Vishal
A 29-year-old male brick-layer presented with a 5-month history of atraumatic right anterolateral shoulder pain and swelling. Pain was present at night and rest but did not prevent him from working. He had no significant medical history. He was a smoker and non-diabetic. On examination, his right shoulder was swollen with minimal irritability but a limited abduction range. His neurological examination showed normal tone, power, proprioception, sensation and reflexes of the upper and lower limbs. X-ray showed an aggressive, lytic appearance of the proximal humerus and glenoid (figure 1). MRI confirmed a destructive lesion involving both sides of the joint with a large, thick walled fluid filled cavity (figure 2).A nuclear medicine scan was performed to further assess whether the lytic lesion was isolated or widespread. Localised high activity suggested an isolated right shoulder arthropathy. Blood test investigations demonstrated C reactive protein< 2 (normal< 5) and a white-cell count of 8.5 (normal 4–10). A syphilis screen, B12, folate, HBA1c and serum electrophoresis were normal. A fine needle aspirate of joint fluid demonstrated no malignant tumour cells, no crystals and a negative culture for organisms. Further MRI of the whole spine revealed an extensive syringomyelia extending from C2-T10 (figure 3), with a basilar herniation of the cerebellum consistent with a type 1 Chiari malformation. Neuropathic (Charcot) arthropathy is a rare degenerative process secondary to a loss of innervation to a joint, causes of which include diabetes, Chiari malformation, end stage renal disease, tabes dorsalis, leprosy, traumatic spinal cord injury and multiple sclerosis. Shoulder neuropathic arthropathy