Functional müllerian tissue within the conus medullaris generating cyclical neurological morbidity in an otherwise healthy female
This case report describes spinal müllerianosis within the conus medullaris, presenting with cyclical neurological symptoms, ultimately requiring surgical resection for diagnosis and treatment.
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This paper is a single-case report describing functional müllerian tissue (intraspinal müllerianosis) located within the conus medullaris in an otherwise healthy female, with an emphasis on gynecological and neurosurgical perspectives and a neurogenetic alternative explanation for etiology. The authors report that the patient experienced cyclical neurological symptoms over several years while being managed symptomatically with an intracystic drain and subcutaneous reservoir, and that surgical resection was ultimately required, which both aided diagnosis and subsequent management. A key limitation is that the work describes only one patient and does not establish causality or definitive origin, noting that the exact etiology remains unclear. Relevance to endometriosis: the authors frame intraspinal müllerianosis as a rare manifestation linked to endometriosis-like müllerian tissue processes and propose it as a differential diagnosis for intraspinal lesions with hemorrhage presenting alongside cyclical symptoms, though the paper’s main focus is a specific conus medullaris case of intraspinal müllerianosis.
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References (22)
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- Intraspinal endometriosis: a case report. via openalex
- Management of intramedullary endometriosis of the conus medullaris. A case report. via openalex
- Müllerianosis. via openalex
- Mullerianosis of the Mesosalpinx: A Case Report via openalex
- Radicular Compression by extradural spinal endometriosis. Case report via openalex
- Recurrent subarachnoid hemorrhage due to endometriosis via openalex
- Secondary müllerian system and endometriosis via openalex
- Spinal intradural müllerianosis: a case report. via openalex
- Uterus-Like Mass in Association with Neural Tube Defect: A Case Report and Review of the Literature via openalex
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