Suri V, Singh Abhijai, Das Reena, Das Ashim, Malhotra P, Jain S, Kumari S, Khandelwal N, Varma S
Department of Internal Medicine, Post Graduate Institute of Medical Education and Research (PGIMER), Chandigarh, 160012, India,
Rheumatol Int. 2014 Apr;34(4):579-82. doi: 10.1007/s00296-013-2752-x. Epub 2013 Apr 23.
Sarcoidosis bone is uncommon, and involvement of the skull is exceptionally rare. We present a 65-year-old obese female who presented with a 2-month history of dryness of mouth, polyuria, fatigue, and anorexia. She had generalized lymphadenopathy, organomegaly, and hypercalcemia, and a skeletal survey revealed extensive osteolytic lesions in the skull and phalanges. Both lymph node biopsy from the cervical lymph node and bone marrow examination revealed non-caseating granulomas, suggesting sarcoidosis. She was started on 1 mg/kg oral corticosteroids; during a follow-up of 6 months, she achieved normocalcemia; however, the punched-out lesions in the skull remained unchanged. This case reiterates several important issues that all lymphadenopathy in emerging nations may not be tubercular, and presence of osteolytic lesions in skull are unusual for sarcoid, at an elderly age, necessitates evaluation for more common etiologies like metastases and myeloma. Finally, patients with osseous sarcoid should be on a close follow-up since due to the rarity of this presentation, no definite consensus on the management of such cases exists in the literature.
结节病累及骨骼并不常见,累及颅骨则极为罕见。我们报告一例65岁肥胖女性,有2个月的口干、多尿、乏力和厌食病史。她有全身淋巴结肿大、脏器肿大和高钙血症,骨骼检查显示颅骨和指骨有广泛的溶骨性病变。颈部淋巴结活检及骨髓检查均发现非干酪样肉芽肿,提示结节病。给予她口服1 mg/kg皮质类固醇;在6个月的随访中,她的血钙恢复正常;然而,颅骨上的筛孔状病变并无变化。该病例重申了几个重要问题,新兴国家所有的淋巴结肿大不一定都是结核性的,老年人颅骨出现溶骨性病变对结节病来说并不常见,需要评估更常见的病因,如转移瘤和骨髓瘤。最后,骨结节病患者应密切随访,因为由于这种表现罕见,文献中对此类病例的治疗尚无明确共识。