The Journal of the Korean Rheumatism Association 2006; 13(4): 311-315
Published online December 30, 2006
© Korean College of Rheumatology
오지선·권귀영*·소민욱·최성호·김용길·나성수·이창근·문희범·유빈
울산대학교 의과대학 서울아산병원 내과학교실, 병리학교실*
Correspondence to : Bin Yoo
Plasma cell granuloma, a form of inflammatory pseudotumor, is a rare nonneoplastic lesion that is characterized by cellular proliferation composed predominantly of polyclonal plasma cells with other inflammatory cells in fibrovascular background. We have experienced an unusual case of plasma cell granuloma of skull that developed in a patient with systemic lupus erythematosus (SLE). A 42-year-old female diagnosed with SLE 13 years ago has complained of palpable scalp mass and headache beginning ten days previously. A brain magnetic resonance imaging showed intensely enhanced soft tissue mass with focal bone defect in right parietal bone and whole body positron emission tomography suggested high possibility of malignancy. Surgical tumor removal was performed. Biopsy specimen revealed inflammatory proliferation predominantly with mature plasma cells which were determined to be polyclonal in immunostaining. Currently, 4 months after surgery, the patient are on regular follow-up with oral medications (prednisolone, hydroxychloroquine) for SLE without evidence of recurrence.
Keywords Plasma cell granuloma, Skull, Systemic lupus erythematosus
The Journal of the Korean Rheumatism Association 2006; 13(4): 311-315
Published online December 30, 2006
Copyright © Korean College of Rheumatology.
오지선·권귀영*·소민욱·최성호·김용길·나성수·이창근·문희범·유빈
울산대학교 의과대학 서울아산병원 내과학교실, 병리학교실*
Ji Seon Oh, M.D., Gui Young Kwon, M.D.*, Min Wook So, M.D., Seong-Ho Choi, M.D., Yong Gil Kim, M.D., Seong-Su Nah, M.D., Chang-Keun Lee, M.D., Hee-Bom Moon, M.D., Bin Yoo, M.D.
Departments of Internal Medicine, Pathology*, Asan Medical Center, University of Ulsan College of Medicine, Seoul, Korea
Correspondence to:Bin Yoo
Plasma cell granuloma, a form of inflammatory pseudotumor, is a rare nonneoplastic lesion that is characterized by cellular proliferation composed predominantly of polyclonal plasma cells with other inflammatory cells in fibrovascular background. We have experienced an unusual case of plasma cell granuloma of skull that developed in a patient with systemic lupus erythematosus (SLE). A 42-year-old female diagnosed with SLE 13 years ago has complained of palpable scalp mass and headache beginning ten days previously. A brain magnetic resonance imaging showed intensely enhanced soft tissue mass with focal bone defect in right parietal bone and whole body positron emission tomography suggested high possibility of malignancy. Surgical tumor removal was performed. Biopsy specimen revealed inflammatory proliferation predominantly with mature plasma cells which were determined to be polyclonal in immunostaining. Currently, 4 months after surgery, the patient are on regular follow-up with oral medications (prednisolone, hydroxychloroquine) for SLE without evidence of recurrence.
Keywords: Plasma cell granuloma, Skull, Systemic lupus erythematosus
Bong-Woo Lee, M.D., Eui-Jong Kwon, M.D., Ji Hyeon Ju, M.D., Ph.D.
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