Roever A C, Rickes S, Flath B, Possinger K
Medizinische Klinik mit Schwerpunkt Onkologie und Hämatologie, Universitätsklinikum Charité, Campus Mitte, Humboldt-Universität zu Berlin.
Dtsch Med Wochenschr. 2004 Feb 27;129(9):434-6. doi: 10.1055/s-2004-820064.
A 59-year-old woman was diagnosed as having solitary bone plasmacytoma of the sternum which was resected. Five month later she presented with a pathological fracture of the clavicle. On examination she had a ptosis and an ophthalmoplegia.
A mass in the clivus extending into the left sphenoid sinus as well as multiple osteolytic lesions in the skull were shown by cranial MRI. Skeletal survey showed multiple osteolytic lesions. Laboratory test did not show any specific abnormalities.
DIAGNOSIS, TREATMENT AND COURSE: The biopsy taken from the mass at the sphenoid sinus demonstrated plasmacytoma. The diagnosis of multiple myeloma was based on the histological evidence of plasmacytoma and the occurrence of multiple lytic bone lesions although no infiltration of bone marrow and none of the specific laboratory findings were present. The patient underwent local radiotherapy with 30 Gy followed by systemic chemotherapy. The symptoms regressed completely under this therapy.
Various cranial nerve syndromes such as the superior orbital fissure syndrome are most often caused by tumors at the skull base. Knowledge of the histological entity is essential for the correct diagnosis and the appropriate therapy because rare tumors like multiple myeloma may also cause such syndromes.
一名59岁女性被诊断为胸骨孤立性骨浆细胞瘤,已行切除手术。五个月后,她出现锁骨病理性骨折。检查发现她有上睑下垂和眼肌麻痹。
头颅MRI显示斜坡有一肿块延伸至左侧蝶窦,颅骨有多处溶骨性病变。骨骼检查显示多处溶骨性病变。实验室检查未发现任何特异性异常。
诊断、治疗与病程:取自蝶窦肿块的活检显示为浆细胞瘤。尽管没有骨髓浸润且无任何特异性实验室检查结果,但基于浆细胞瘤的组织学证据和多处溶骨性骨病变的出现,诊断为多发性骨髓瘤。患者接受了30 Gy的局部放疗,随后进行全身化疗。在此治疗下症状完全消退。
各种颅神经综合征,如眶上裂综合征,最常见的病因是颅底肿瘤。了解组织学实体对于正确诊断和适当治疗至关重要,因为像多发性骨髓瘤这样的罕见肿瘤也可能导致此类综合征。