Turner Matthew D, Goodale Elicia, Gibney Barry C, Reyes Maria Cecilia D
College of Medicine, Medical University of South Carolina, Charleston, South Carolina, USA.
Department of Pathology, Medical University of South Carolina, Charleston, South Carolina, USA.
Int J Surg Pathol. 2023 Jun;31(4):431-434. doi: 10.1177/10668969221105619. Epub 2022 Jun 14.
Sixteen years since their initial description in the literature, posterior mediastinal Mullerian cysts - otherwise known as cysts of Hattori, after their discoverer - remain rare, with only 40 patients reported as of 2020. We report a 43 year old obese female that presented with a 2.6 cm cyst found in the posterior mediastinum by endoscopic ultrasound (EUS) and previously by chest magnetic resonance imaging (MRI) originally diagnosed as a congenital enteric duplication cyst of the esophagus radiologically. Upon surgical excision via a DaVinci thoracoscopy, the cyst was confirmed to be of Mullerian origin by PAX8, WT1, and ER staining. It is possible that the majority of cysts of Hattori remain unrecognized and undiagnosed, given their rarity and resemblance to other pathologies. It is important that this entity become a part of every pathologist's differential for a posterior mediastinal cyst in a female.
自后纵隔苗勒氏囊肿(以其发现者命名为服部囊肿)首次在文献中被描述以来,已经过去16年了,这类囊肿仍然很罕见,截至2020年仅有40例患者的报道。我们报告了一名43岁的肥胖女性,她通过内镜超声(EUS)在纵隔后部发现了一个2.6厘米的囊肿,此前胸部磁共振成像(MRI)最初将其诊断为食管先天性肠重复囊肿。经达芬奇胸腔镜手术切除后,通过PAX8、WT1和雌激素受体(ER)染色证实该囊肿起源于苗勒氏管。鉴于其罕见性以及与其他病变的相似性,大多数服部囊肿可能仍未被识别和诊断。对于女性后纵隔囊肿,将这一实体纳入每位病理学家的鉴别诊断范围很重要。