2011
DOI: 10.1007/s00296-011-2100-y
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Sarcoidosis and sacroiliitis, a case report

Abstract: Sarcoidosis is a multisystem disorder of unknown etiology characterized by the presence of non-caseating granulomas in the organs affected. Sarcoid arthropathy is a rare manifestation, and sacroiliitis is an unusual first manifestation of the disorder

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Cited by 6 publications
(3 citation statements)
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“…There are rare reports of sarcoidosis coexisting with spondyloarthropathy [36, 42, 43]. Biopsy of the SI joint in sarcoid cases demonstrates non-caseating granulomata in the synovium [44, 45]; however, non-specific inflammatory changes have been described [39]. Even with biopsy changes consistent with sarcoid, tuberculous infection must be ruled out as well.…”
Section: Discussionmentioning
confidence: 99%
“…There are rare reports of sarcoidosis coexisting with spondyloarthropathy [36, 42, 43]. Biopsy of the SI joint in sarcoid cases demonstrates non-caseating granulomata in the synovium [44, 45]; however, non-specific inflammatory changes have been described [39]. Even with biopsy changes consistent with sarcoid, tuberculous infection must be ruled out as well.…”
Section: Discussionmentioning
confidence: 99%
“…Fever is usually absent or low grade • Risk factors: IV drug use, pelvic trauma, infectious endocarditis, immunosuppression, cutaneous or genitourinary infection • Imaging: on MRI, unilateral periarticular muscle edema, thick capsulitis, and extracapsular fluid collection may be useful in differentiating infectious sacroiliitis from sacroiliitis due to axSpA Whipple disease [152][153][154][155][156][157][158][159][160][161] • Large joint migratory arthralgias, abdominal pain, weight loss, and diarrhea, with or without IBP • Risk factors: occupational exposure to soil or animals • Imaging: sacroiliitis and spondylitis indistinguishable from axSpA Familial Mediterranean fever 143,[162][163][164] • Intermittent fevers, abdominal pain, large joint arthritis, enthesitis, IBP. Childhood or adolescent onset is typical, but may occur in adulthood • Risk factors: genetics (MEFV gene mutations); Turkish, Armenian, North African, Jewish, and Arab descent • Imaging: sacroiliitis indistinguishable from axSpA Sarcoidosis 149,[165][166][167][168][169][170] • IBP • Risk factors: sacroiliitis may occur most frequently in sarcoidosis limited to the thorax (thoracic lymph nodes and lungs) • Imaging: sacroiliitis indistinguishable from axSpA Spinal calcium pyrophosphate deposition disease [171][172][173] • Periodic IBP with elevated inflammatory markers • Risk factors: widespread peripheral chondrocalcinosis • Imaging: linear calcium deposition in intervertebral disks, SIJs, and/or peripheral joints Idiopathic hypoparathyroidism [174][175][176][177][178] • Hypocalcemia presentation ± back pain experience little or no pain relief with NSAIDs. 123 Furthermore, the sites of maximal point tenderness with fibromyalgia are usually not located precisely at entheseal sites.…”
Section: Fibromyalgiamentioning
confidence: 99%
“…Sacroiliac joint involvement in sarcoidosis often occurs with a history of IBP but may present in patients with mechanical back pain 149,168 . Radiographic evidence of sacroiliitis in sarcoidosis may be similar to that of AS; a biopsy of the SIJ may reveal noncaseating granulomata in the synovium, but SIJ biopsy is usually unnecessary if a sarcoidosis diagnosis can be made via clinical presentation or biopsy of extra-articular tissue 169 . Sacroiliitis may occur most frequently in sarcoidosis limited to the thorax 170 …”
Section: Sarcoidosismentioning
confidence: 99%