TY - JOUR
T1 - Experience with surgery for thymoma associated with pure red blood cell aplasia. Report of three cases
AU - Fujimura, S.
AU - Kondo, T.
AU - Yamauchi, A.
AU - Handa, M.
AU - Nakada, T.
N1 - Funding Information:
Supported in part by Japan Welfare Ministry Board (58–32).
PY - 1985
Y1 - 1985
N2 - We present three cases of thymoma associated with pure red blood cell aplasia in which thymomectomy and thymectomy were performed. Case 1, a patient with pure red blood cell aplasia and hypogammaglobulinemia, was treated after surgery with immunosuppressive agents. She did not show any remission and died eight months after the operation. Case 2, a patient with pure red blood cell aplasia alone, showed transient erythropoiesis only in the early postoperative period and died one year and seven months after the operation. Patient 3 had pure red blood cell aplasia alone before surgery and was treated after surgery with prednisolone and fluoxymesterone. He showed good remission from the aplasia after these treatments; however, myasthenia gravis appeared seven months after the operation. These results seem to show that such combined therapy as applied in case 3 may be effective for some of the patients with pure red blood cell aplasia and thymoma; however, the effects of thymomectomy or thymectomy (or both) are still controversial for the treatment of pure red blood cell aplasia.
AB - We present three cases of thymoma associated with pure red blood cell aplasia in which thymomectomy and thymectomy were performed. Case 1, a patient with pure red blood cell aplasia and hypogammaglobulinemia, was treated after surgery with immunosuppressive agents. She did not show any remission and died eight months after the operation. Case 2, a patient with pure red blood cell aplasia alone, showed transient erythropoiesis only in the early postoperative period and died one year and seven months after the operation. Patient 3 had pure red blood cell aplasia alone before surgery and was treated after surgery with prednisolone and fluoxymesterone. He showed good remission from the aplasia after these treatments; however, myasthenia gravis appeared seven months after the operation. These results seem to show that such combined therapy as applied in case 3 may be effective for some of the patients with pure red blood cell aplasia and thymoma; however, the effects of thymomectomy or thymectomy (or both) are still controversial for the treatment of pure red blood cell aplasia.
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U2 - 10.1378/chest.88.2.221
DO - 10.1378/chest.88.2.221
M3 - Article
C2 - 4017676
AN - SCOPUS:0021843732
SN - 0012-3692
VL - 88
SP - 221
EP - 225
JO - Diseases of the chest
JF - Diseases of the chest
IS - 2
ER -