Okuno Noriko, Takagi Kohji, Nakajima Takahiko, Fujinami Haruka, Hirabayashi Kenichi, Sasahara Masakiyo
Department of Pathology, Faculty of Medicine, Academic Assembly, University of Toyama, Toyama, JPN.
Department of Diagnostic Pathology, Toyama University Hospital, Toyama, JPN.
Cureus. 2024 Sep 22;16(9):e69907. doi: 10.7759/cureus.69907. eCollection 2024 Sep.
Alveolar rhabdomyosarcoma (ARMS) is a malignant tumor with skeletal muscle differentiation that usually occurs in soft tissues of the extremities or trunk. To date, only a few cases of primary gastric ARMS have been reported. Herein, we describe a case of ARMS in a man in his 80s and present a literature review. A submucosal tumor-like lesion was detected endoscopically. Histologically, the tumor cells exhibited a poorly differentiated morphology with hyperchromatic nuclei. Neuroendocrine markers, such as synaptophysin and CD56, were positive, and neuroendocrine carcinoma (NEC) was considered a differential diagnosis. However, both myogenic markers and OLIG2, which reflect FAX3 or FAX7 fusion, were positive, leading to a diagnosis of ARMS. Primary gastric ARMS is an extremely rare condition. Better awareness of this entity and its similarity to NEC is necessary for appropriate diagnosis and treatment.
肺泡状横纹肌肉瘤(ARMS)是一种具有骨骼肌分化的恶性肿瘤,通常发生于四肢或躯干的软组织。迄今为止,仅报道过少数原发性胃ARMS病例。在此,我们描述了一例80多岁男性的ARMS病例,并进行文献综述。内镜检查发现一个黏膜下肿瘤样病变。组织学上,肿瘤细胞表现出分化不良的形态,核染色质增多。神经内分泌标志物,如突触素和CD56呈阳性,神经内分泌癌(NEC)被考虑作为鉴别诊断。然而,反映FAX3或FAX7融合的肌源性标志物和OLIG2均呈阳性,从而诊断为ARMS。原发性胃ARMS是一种极其罕见的疾病。为了进行恰当的诊断和治疗,有必要更好地认识这种疾病及其与NEC的相似性。