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与骨髓增生异常综合征相关的阑尾髓外造血:一例报告

Extramedullary Hematopoiesis in the Appendix Associated With Myelodysplastic Syndrome: A Case Report.

作者信息

Kinjo Naoki, Satoshi Matsukuma, Suzuki Atomu, Yamashita Koji, Yamashita Yoshimi

机构信息

Surgery, Japan Community Healthcare Organization (JCHO) Tokuyama Central Hospital, Shunan, JPN.

Gastrointestinal Surgery, Japan Community Healthcare Organization (JCHO) Tokuyama Central Hospital, Shunan, JPN.

出版信息

Cureus. 2025 Feb 24;17(2):e79560. doi: 10.7759/cureus.79560. eCollection 2025 Feb.

Abstract

Extramedullary hematopoiesis (EMH) is characterized by the presence of hematopoietic tissue outside the bone marrow, more commonly in the liver and the spleen. However, there are very few reports of nonhepatosplenic extramedullary hematopoiesis (NHS-EMH). Among the NHS-EMHs, NHS-EMH in the appendix is extremely uncommon. We hereby present a case of appendiceal NHS-EMH and discuss it with a literature review. The patient was a gentleman in his 70s who had been treated for follicular lymphoma seven years ago. He gradually developed leukopenia and six months ago was diagnosed with myelodysplastic syndrome (MDS). Four days prior to admission, he developed abdominal pain that was localized to the right lower quadrant and was accompanied by fever and loss of appetite. Abdominal CT revealed a thickening of the appendiceal wall and increased fat density around it. A diagnosis of acute appendicitis was made, and he was treated conservatively. However, his condition did not improve, and a laparoscopic appendectomy was performed. Diffuse proliferation of hematopoietic cells in the submucosal layer of the appendix was observed on histopathological examination. This confirmed the diagnosis of NHS-EMH. The postoperative course was uneventful; however, the patient's MDS progressed to acute leukemia in the next four months, and he died 14 months after surgery. Appendiceal NHS-EMH is an extremely rare condition associated with clinical features that are similar to those of acute appendicitis, making preoperative diagnosis challenging. Temporary symptom control could be achieved with an appendectomy.

摘要

髓外造血(EMH)的特征是骨髓外存在造血组织,更常见于肝脏和脾脏。然而,关于非肝脾性髓外造血(NHS-EMH)的报道非常少。在NHS-EMH中,阑尾的NHS-EMH极为罕见。我们在此报告一例阑尾NHS-EMH病例,并结合文献进行讨论。患者为一名70多岁的男性,七年前曾接受滤泡性淋巴瘤治疗。他逐渐出现白细胞减少,六个月前被诊断为骨髓增生异常综合征(MDS)。入院前四天,他出现右下象限局限性腹痛,并伴有发热和食欲不振。腹部CT显示阑尾壁增厚,周围脂肪密度增加。诊断为急性阑尾炎,对其进行了保守治疗。然而,他的病情并未改善,遂进行了腹腔镜阑尾切除术。组织病理学检查发现阑尾黏膜下层造血细胞弥漫性增生。这证实了NHS-EMH的诊断。术后过程顺利;然而,患者的MDS在接下来的四个月进展为急性白血病,术后14个月死亡。阑尾NHS-EMH是一种极为罕见的疾病,其临床特征与急性阑尾炎相似,术前诊断具有挑战性。阑尾切除术可实现症状的临时控制。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2740/11939031/e6514e7d95f0/cureus-0017-00000079560-i01.jpg

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