Umino T, Ohdama S, Sawada M, Tachibana S, Takano S, Miyake S, Aoki N, Yamamoto N, Matsubara O, Masuda S
First Department of Internal Medicine, Tokyo Medical and Dental University, Japan.
Nihon Kyobu Shikkan Gakkai Zasshi. 1993 Aug;31(8):1012-8.
A 69-year-old woman was hospitalized because of abnormal lung shadow and IgG-lambda paraproteinemia. She was otherwise healthy and asymptomatic. Chest roentgenogram showed a consolidation in the right lower lobe. Chest CT showed a tumour in S8 and subpleural interstitial shadow in S10. No intrathoracic lymphadenopathy was found. Serum IgG was 6,109 mg/dl. The cell count obtained by bronchoalveolar lavage (BAL) was 44.5% plasma cells and 17.5% lymphocytes. CD19-positive lymphocytes were prominent. The IgG/albumin ratio was 13 times higher, and IL-6/albumin ratio was 29 times higher in lavage fluid than in serum. Transbronchial lung biopsy (TBLB) specimen showed interstitial infiltration of plasma cells and lymphocytes. Right lower lobectomy was performed, and serum IgG subsequently decreased to about 4,000 mg/dl. DNA was extracted from the surgical specimen, and analyzed by Polymerase Chain Reaction (PCR) method. A rearrangement band was amplified with Fr3a & VLJH primers (immunoglobulin heavy chain gene). The infiltrated cells were proved to be monoclonal B-cells. This case was diagnosed as small lymphocytic lymphoma, plasmacytoid. Most primary pulmonary lymphomas are well differentiated B-cell type, and the histopathological findings resemble those of LIP or pseudolymphoma. Gene analysis may thus be an effective procedure for the distinction between inflammatory and neoplastic cell proliferation, such as LIP and lymphoma.
一名69岁女性因肺部阴影异常和IgG-λ副蛋白血症入院。她其他方面健康且无症状。胸部X线片显示右下叶实变。胸部CT显示S8区有肿瘤,S10区有胸膜下间质阴影。未发现胸内淋巴结肿大。血清IgG为6109mg/dl。经支气管肺泡灌洗(BAL)获得的细胞计数显示浆细胞占44.5%,淋巴细胞占17.5%。CD19阳性淋巴细胞突出。灌洗液中IgG/白蛋白比值比血清高13倍,IL-6/白蛋白比值比血清高29倍。经支气管肺活检(TBLB)标本显示浆细胞和淋巴细胞间质浸润。行右下叶切除术,随后血清IgG降至约4000mg/dl。从手术标本中提取DNA,并用聚合酶链反应(PCR)方法进行分析。用Fr3a和VLJH引物(免疫球蛋白重链基因)扩增出一条重排带。证实浸润细胞为单克隆B细胞。该病例诊断为浆细胞样小淋巴细胞淋巴瘤。大多数原发性肺淋巴瘤为高分化B细胞型,组织病理学表现类似于淋巴细胞间质性肺炎(LIP)或假性淋巴瘤。因此,基因分析可能是区分LIP和淋巴瘤等炎症性和肿瘤性细胞增殖的有效方法。