Bianchi Rita, Fraternali Orcioni Giulio, Spina Bruno, Vellone Valerio Gaetano, Ravetti Jean Luis, Gaggero Gabriele
Unit of Pathology, Ospedale di Sestri Levante, ASL4, Genoa, Italy.
Unit of Pathology, Ospedali Santi Croce e Carle, Cuneo, Italy.
Pathologica. 2022 Apr;114(2):159-163. doi: 10.32074/1591-951X-266.
Microcystic/reticular (MRV) schwannoma has been described since 2008, but remains a rarely encountered entity. MRV has a predilection for visceral locations and has variable histologic appareances. Given its rarity and anatomic variability, this entity could raise differential diagnostic issues with other tumours and malignancies. We describe the case of a 69-year-old male followed at IRCCS Ospedale Policlinico San Martino of Genoa for his previous history of non-Hodgkin lymphoma. A para-aortic mass was discovered during follow-up, which -due to its stability, also after chemotherapy- had been hypothesized to be a non-lymphomatous lesion; given the dimensions and the site, the mass was removed. Histological evaluation showed a nodule limited by a slight fibrous capsule and characterized by a proliferation of medium-sized fusiform cells, with elongated nuclei and scarce eosinophilic cytoplasm. Given the lack of malignant signs and the strong expression of protein S-100, a diagnosis of mesenchymal neoplasia with expression of neural markers compatible with reticular schwannoma was made. The neoplasm has not recurred since its removal. The case we present is, at our best knowledge, the first described in the retroperitoneum, a site where the exclusion of other mesenchymal malignancies is mandatory. The rarity and variability of presentations could create problems of differential diagnosis both with mucinous-producing carcinomas or with other soft tissue tumours, with myxoid or reticular structure. The description of this case could help raise information on this rare neoplasm and help distinguish it from other malignancies, especially in unusual sites.
微囊型/网状(MRV)神经鞘瘤自2008年以来已有描述,但仍然是一种罕见的实体。MRV好发于内脏部位,组织学表现多样。鉴于其罕见性和解剖学变异性,该实体可能会引发与其他肿瘤和恶性肿瘤的鉴别诊断问题。我们描述了一名69岁男性的病例,该患者因既往非霍奇金淋巴瘤病史在热那亚的IRCCS圣马尔蒂诺综合医院接受随访。随访期间发现一个主动脉旁肿块,由于其在化疗后仍保持稳定,曾被推测为非淋巴瘤性病变;鉴于肿块的大小和部位,将其切除。组织学评估显示一个结节,周围有轻微的纤维性包膜,其特征为中等大小的梭形细胞增生,细胞核细长,嗜酸性细胞质稀少。鉴于缺乏恶性征象且蛋白S - 100强表达,做出了诊断为具有神经标志物表达的间叶性肿瘤,符合网状神经鞘瘤。该肿瘤切除后未复发。据我们所知,我们所呈现的病例是首次在腹膜后描述的,在这个部位必须排除其他间叶性恶性肿瘤。其表现的罕见性和变异性可能会在与黏液腺癌或其他具有黏液样或网状结构的软组织肿瘤进行鉴别诊断时产生问题。对该病例的描述有助于增加关于这种罕见肿瘤的信息,并有助于将其与其他恶性肿瘤区分开来,特别是在不寻常的部位。