Tzilves D, Gatopoulou A, Zervas K, Katodritou E, Patakiouta F, Tarpagos A, Katsos I
Department of Gastroenterology, Theagenio Cancer Hospital, 2, Al. Simeonidi 54007, Thessaloniki, Greece.
World J Gastroenterol. 2007 Apr 7;13(13):2011-3. doi: 10.3748/wjg.v13.i13.2011.
Gastrointestinal stromal tumors (GISTs) are rare tumors, which represent approximately 1% of the neoplasms of the gastrointestinal tract. These tumors rarely give extra-abdominal metastases. However, their clinical outcome is potentially adverse. In some rare cases, co-existance of GISTs with other malignancies has been reported. Here we present a case of a 74-year old male with GIST, which was managed by surgical resection. Fourteen months later, the patient presented with liver metastases and imatinib mesylated was administered. During treatment, the patient reported skeletal pain and plane X-rays revealed osteolytic bone lesions. Further investigation revealed the presence of multiple myeloma. To the best of our knowledge, this is the first report of the co-existence of multiple myeloma (MM) with GIST.
胃肠道间质瘤(GISTs)是罕见肿瘤,约占胃肠道肿瘤的1%。这些肿瘤很少发生腹外转移。然而,其临床预后可能较差。在一些罕见病例中,已有GISTs与其他恶性肿瘤共存的报道。在此,我们报告一例74岁男性GIST患者,通过手术切除进行治疗。14个月后,患者出现肝转移并接受甲磺酸伊马替尼治疗。治疗期间,患者诉说骨骼疼痛,X线平片显示溶骨性骨病变。进一步检查发现存在多发性骨髓瘤。据我们所知,这是首例多发性骨髓瘤(MM)与GIST共存的报告。