Corpechot C, Lémann M, Brocheriou I, Mariette X, Bonnet J, Daniel M T, Bertheau P, Lavergne A, Modigliani R
Service de Gastroentérologie, Hôpitaux Saint-Louis and Lariboisière, Paris, France.
Am J Gastroenterol. 1998 Dec;93(12):2586-8. doi: 10.1111/j.1572-0241.1998.00726.x.
We report the case of a 40-yr-old man presenting with symptoms of small bowel obstruction. Small bowel x-rays revealed a stricture of the mid-jejunum. Push enteroscopy found a polypoid mass at 1 meter of the ligament of Treitz. Histopathological examination of the biopsy and surgical specimens showed a diffuse infiltrate of the mucosa made of medium to large cells, which were stained on immunohistochemistry by the leucocyte marker CD45 and the histiocyte/monocyte marker CD68 but were negative for the B and T cell markers. Cytological examination of the ascitic fluid revealed many myelobasts with cytoplasmic Auer rods and positive myeloperoxidase staining. There was no evidence of blood or bone marrow involvement suggestive of acute leukemia or myeloproliferative disorders. These findings were consistent with the diagnosis of preleukemic granulocytic sarcoma (or chloroma). Chemotherapy led to complete remission, but 21 months later the patient developed an acute myeloid leukemia. He died from aspergillus pneumonitis, 10 months after bone marrow allograft. Preleukemic granulocytic sarcoma of the small bowel is a rare condition and its diagnosis is usually not easy, requiring histochemical or immunohistochemical studies. Most cases have progressed to acute myeloid leukemia.
我们报告了一例40岁男性出现小肠梗阻症状的病例。小肠X线检查显示空肠中段狭窄。推进式小肠镜检查发现在屈氏韧带1米处有一个息肉样肿物。活检及手术标本的组织病理学检查显示黏膜有由中到大细胞组成的弥漫性浸润,免疫组织化学染色显示这些细胞被白细胞标志物CD45和组织细胞/单核细胞标志物CD68染色,但B细胞和T细胞标志物呈阴性。腹水的细胞学检查发现许多有细胞质奥氏小体且髓过氧化物酶染色阳性的髓母细胞。没有证据表明存在提示急性白血病或骨髓增殖性疾病的血液或骨髓受累情况。这些发现与白血病前期粒细胞肉瘤(或绿色瘤)的诊断相符。化疗导致完全缓解,但21个月后患者发展为急性髓系白血病。骨髓同种异体移植10个月后,他死于曲霉菌性肺炎。小肠白血病前期粒细胞肉瘤是一种罕见疾病,其诊断通常并不容易,需要进行组织化学或免疫组织化学研究。大多数病例已进展为急性髓系白血病。