Sakuma Hidenori, Okabe Mitsukuni, Yokoi Motoo, Eimoto Tadaaki, Inagaki Hiroshi
Department of Pathology, Nagoya City University Graduate School of Medical Sciences, Nagoya, Japan.
Pathol Int. 2006 Jun;56(6):331-5. doi: 10.1111/j.1440-1827.2006.01967.x.
Mucosa-associated lymphoid tissue (MALT) lymphoma presentation in the oral cavity is very rare. Reported herein is a case of intraoral MALT lymphoma of the minor salivary gland in a 70-year-old woman with Sjogren's syndrome. Unexpectedly, a spontaneous clinically and histologically confirmed regression occurred 1 month after the tumor biopsy for diagnosis. Considering that salivary MALT lymphoma is associated with Sjogren's syndrome and that the chronic inflammation caused by Sjogren's syndrome persisted, it is hypothesized that the tumor clone might be present in the regressed lesion. Minimal residual tumor clone identical with the primary lesion was detected using the polymerase chain reaction (PCR) clonality assay for immunoglobulin heavy chain gene (IgH) rearrangement. No recurrence was clinically evident 38 months after the diagnosis. Spontaneous regression of MALT lymphoma should be examined at the molecular level in addition to clinical and histological evaluations. When minimal residual disease is detected, close follow up is necessary for early detection of the tumor relapse.
黏膜相关淋巴组织(MALT)淋巴瘤在口腔的表现非常罕见。本文报道了一例70岁患干燥综合征女性的小唾液腺口腔内MALT淋巴瘤病例。出乎意料的是,在肿瘤活检确诊1个月后出现了临床和组织学证实的自发消退。鉴于唾液腺MALT淋巴瘤与干燥综合征相关且干燥综合征引起的慢性炎症持续存在,推测肿瘤克隆可能存在于消退的病变中。使用免疫球蛋白重链基因(IgH)重排的聚合酶链反应(PCR)克隆性分析检测到与原发病变相同的微小残留肿瘤克隆。诊断后38个月临床上未发现复发。除了临床和组织学评估外,还应在分子水平上检查MALT淋巴瘤的自发消退情况。当检测到微小残留病时,需要密切随访以便早期发现肿瘤复发。