Scott William W, Ray Bappaditya, Rickert Kim L, Madden Christopher J, Raisanen Jack M, Mendelsohn Dianne, Rogers David, Whitworth Tony A
Department of Neurosurgery, University of Texas Southwestern Medical Center, 5323 Harry Hines Blvd., Dallas, TX, 75390-8855, USA,
Childs Nerv Syst. 2014 Apr;30(4):717-21. doi: 10.1007/s00381-013-2291-5. Epub 2013 Oct 1.
Endometriosis is a common disease; however, ectopic müllerian tissue within the spine is a rare entity with the potential for producing significant neurological compromise. There are several postulated etiologies for this phenomenon, and only a few case reports are available in the world literature. Knowledge of this rare phenomenon is of paramount importance, since early diagnosis can lead to lessened neurological morbidity.
In this manuscript, we present a case report, discuss gynecological and neurosurgical perspectives relating to the treatment strategies for managing this entity, and propose an alternative explanation for such an occurrence from a neurogenetic standpoint.
We present a case of spinal müllerianosis within the conus medullaris which was managed symptomatically for several years with an intracystic drain and subcutaneous reservoir. Over the years, it became clear that there was a cyclical presentation to her clinical malady, which at times was severe. Ultimately, she required surgical resection which aided in her diagnosis and subsequent treatment.
Intraspinal müllerianosis is a rare location for an otherwise common disease in women and has the potential to create significant neurological morbidity by creating a mass lesion. Although the exact etiology remains unclear, the histogenic theories of embryologic origin appear most plausible. Treatment strategies for this condition may include hormonal therapy, obstetrical surgery, or open spinal surgery. This unusual and poorly understood disease should be considered in the differential diagnosis for intraspinal lesions presenting with hemorrhage in the clinical context of cyclical neurological symptoms.
子宫内膜异位症是一种常见疾病;然而,脊柱内的异位苗勒管组织是一种罕见情况,有可能导致严重的神经功能损害。对于这种现象有几种假定的病因,而世界文献中仅有少数病例报告。了解这种罕见现象至关重要,因为早期诊断可降低神经功能损害的发生率。
在本手稿中,我们呈现一例病例报告,讨论与该病症治疗策略相关的妇科和神经外科观点,并从神经遗传学角度对这种情况提出另一种解释。
我们报告一例圆锥内的脊柱苗勒管异位症病例,该病例通过囊内引流和皮下储液器进行了数年的对症治疗。多年来,很明显她的临床病症呈周期性表现,有时还很严重。最终,她需要手术切除,这有助于诊断及后续治疗。
脊柱内苗勒管异位症在女性常见疾病中是一种罕见的发病部位,有可能通过形成肿块病变导致严重的神经功能损害。尽管确切病因仍不清楚,但胚胎起源的组织发生学理论似乎最具合理性。这种病症的治疗策略可能包括激素治疗、产科手术或开放性脊柱手术。在伴有周期性神经症状且有出血表现的脊柱内病变的鉴别诊断中,应考虑这种不寻常且了解较少的疾病。