Ladak Rahman, Magnuson William
Department of Undergraduate Medical Education, Schulich School of Medicine and Dentistry, Western University, London, Ontario, Canada.
Department of Medical Imaging, University of Toronto, Toronto, Ontario, Canada.
Radiol Case Rep. 2024 Jul 20;19(10):4184-4189. doi: 10.1016/j.radcr.2024.06.067. eCollection 2024 Oct.
Polysplenia syndrome is an embryological disorder whereby the usual left-right asymmetry of thoracic and abdominal viscera fails to develop. It is a rare entity, estimated to occur at a frequency of 1 in 40,000, and is often associated with cardiac and biliary abnormalities. More than 75% of patients die before the age of 5 years, and even in the absence of cardiac anomalies, only 5%-10% of patients are expected to survive into adulthood without complications. Although polysplenia syndrome encompasses a wide range of anatomic abnormalities, there is no single pathognomonic feature. Hence, the prognosis of patients with polysplenia depends on their anatomy, thus necessitating radiology in their management. Here we present a case of a 56-year-old man with polysplenia syndrome and situs inversus totalis. This presentation is atypical because polysplenia is usually considered a form of situs ambiguus, and cases with situs inversus totalis are exceedingly rare. Also noted in our patient are variations in the great vessels, including aortic arch branches and the venae cavae which are features not typically associated with either polysplenia syndrome or situs inversus totalis. The patient is healthy and asymptomatic at baseline, with his diagnosis being made incidentally. Our case report is the first to describe this unique combination of cardiothoracic and cardiovascular anatomy. It also emphasizes the importance of radiologists in caring for patients with laterality defects. As these disorders are uncommon, more data on their anatomic variations may help provide better medical care to this patient population.
多脾综合征是一种胚胎发育障碍性疾病,胸腔和腹腔脏器通常的左右不对称发育未能形成。它是一种罕见疾病,估计发病率为四万分之一,常伴有心脏和胆道异常。超过75%的患者在5岁前死亡,即使没有心脏异常,预计也只有5%-10%的患者能无并发症地存活至成年。尽管多脾综合征包含广泛的解剖学异常,但没有单一的特征性表现。因此,多脾综合征患者的预后取决于其解剖结构,这就使得在其治疗过程中需要进行放射学检查。在此,我们报告一例56岁患有多脾综合征及全内脏转位的男性患者。这种表现并不典型,因为多脾通常被认为是内脏反位不明确的一种形式,而全内脏转位的病例极为罕见。在我们的患者中还发现了大血管的变异,包括主动脉弓分支和腔静脉,这些特征通常与多脾综合征或全内脏转位均无关联。该患者基线时健康且无症状,其诊断是偶然发现的。我们的病例报告首次描述了这种独特的心胸和心血管解剖结构组合。它还强调了放射科医生在护理有左右侧缺陷患者中的重要性。由于这些疾病并不常见,更多关于其解剖变异的数据可能有助于为这一患者群体提供更好的医疗护理。