Key Laboratory of Evidence Science, Ministry of Education, China University of Political Science and Law, Beijing, China.
Center of Cooperative Innovation for Judicial Civilization, Beijing, China.
Medicine (Baltimore). 2024 Nov 29;103(48):e40745. doi: 10.1097/MD.0000000000040745.
Individuals diagnosed with neurofibromatosis type I (NF1) commonly present with neurofibromas, and a subset may progress to develop malignant peripheral nerve sheath tumors (MPNST) during their lifetime. Diagnosing and treating MPNST, typically linked to NF1, poses challenges for clinicians due to its histopathological complexity.
A 25-year-old male presented with postprandial discomfort and vomiting, subsequently developing left mid-abdominal pain.
The patient was admitted to the hospital, where a low-density retroperitoneal mass was detected via computed tomography (CT). Histopathological examination revealed spindle-shaped tumor cells characterized by abundant cytoplasm and highly pigmented nuclei, demonstrating pathological nuclear division. The tumor cells exhibited partial cytoplasmic positive for S-100 and focal cytoplasmic positive for cytokeratin (CK) and desmin, as determined by immunohistochemical staining. Genetic analysis of blood and extracted tissues identified an NF1 missense mutation. Prior research corroborated the pathological diagnosis of MPNST exhibiting both epithelial and myogenic differentiation.
A retroperitoneal mass excision was conducted, revealing a mass located in the retroperitoneal omental sac.
Approximately 5 hours after surgery, the patient's blood pressure exhibited a gradual decline. An emergency laparotomy was conducted. Approximately 3000 mL of blood was identified in the upper abdominal cavity. The patient's blood pressure consistently declined and ultimately resulted in death after 2 days.
It is crucial to assess the potential for heterogeneous differentiation in MPNST during pathological diagnosis. In the treatment of MPNST with heterogeneous differentiation, particularly in cases with significant tumor bulk, surgeons must anticipate potential hemorrhagic complications and adopt a cautious approach to surgical intervention.
患有神经纤维瘤病 1 型(NF1)的个体通常会出现神经纤维瘤,其中一部分在其一生中可能进展为恶性外周神经鞘瘤(MPNST)。由于其组织病理学的复杂性,诊断和治疗与 NF1 相关的 MPNST 对临床医生来说是一个挑战。
一名 25 岁男性出现餐后不适和呕吐,随后出现左中腹部疼痛。
患者住院后,通过计算机断层扫描(CT)发现低密度腹膜后肿块。组织病理学检查显示,梭形肿瘤细胞具有丰富的细胞质和高度色素化的核,表现出病理性核分裂。肿瘤细胞的细胞质部分对 S-100 呈阳性,部分对细胞角蛋白(CK)和结蛋白呈阳性,免疫组织化学染色显示。血液和提取组织的基因分析发现 NF1 错义突变。先前的研究证实了具有上皮和肌源性分化的 MPNST 的病理诊断。
进行了腹膜后肿块切除术,显示位于腹膜后网膜囊的肿块。
手术后约 5 小时,患者的血压逐渐下降。进行了紧急剖腹手术。在上腹部发现约 3000 毫升血液。患者的血压持续下降,最终在 2 天后死亡。
在病理诊断中评估 MPNST 异质性分化的潜力至关重要。在治疗具有异质性分化的 MPNST 时,特别是在肿瘤体积较大的情况下,外科医生必须预测潜在的出血性并发症,并谨慎地进行手术干预。