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Limited dorsal myeloschisis associated with intramedullary infantile hemangioma in the conus medullaris: illustrative case

BACKGROUND: Limited dorsal myeloschisis (LDM) and intramedullary infantile hemangioma rarely coexist in the spinal cord. OBSERVATIONS: The authors describe the case of a 3-month-old girl who, despite lacking neurological symptoms or signs, had a cigarette burn-like mark at the lumbosacral area and s...

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Autores principales: Nakanishi, Yoko, Kunihiro, Noritsugu, Umaba, Ryoko, Matsusaka, Yasuhiro, Inoue, Takeshi, Sakamoto, Hiroaki
Formato: Online Artículo Texto
Lenguaje:English
Publicado: American Association of Neurological Surgeons 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10550677/
https://www.ncbi.nlm.nih.gov/pubmed/37096816
http://dx.doi.org/10.3171/CASE22359
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author Nakanishi, Yoko
Kunihiro, Noritsugu
Umaba, Ryoko
Matsusaka, Yasuhiro
Inoue, Takeshi
Sakamoto, Hiroaki
author_facet Nakanishi, Yoko
Kunihiro, Noritsugu
Umaba, Ryoko
Matsusaka, Yasuhiro
Inoue, Takeshi
Sakamoto, Hiroaki
author_sort Nakanishi, Yoko
collection PubMed
description BACKGROUND: Limited dorsal myeloschisis (LDM) and intramedullary infantile hemangioma rarely coexist in the spinal cord. OBSERVATIONS: The authors describe the case of a 3-month-old girl who, despite lacking neurological symptoms or signs, had a cigarette burn-like mark at the lumbosacral area and skin dimpling in the gluteal area. Magnetic resonance imaging showed a low-set conus due to a thickened filum and an abnormal subcutaneous stalk connected to the conus medullaris. In combination with the skin lesions, these findings strongly implied nonsaccular-type LDM. An intramedullary mass in the conus medullaris was also shown on magnetic resonance imaging and was homogenously enhanced with isointensity on T1- and T2-weighted images. We prophylactically untethered the spinal cord and partially removed the intramedullary mass, which had no clear borders, for a safe surgical dissection. Histologically, the intramedullary mass was an infantile hemangioma, and the subcutaneous stalk was a lesion associated with LDM. The patient remained neurologically intact after surgery, and then 2 years later, there was spontaneous regression of the residual tumor. LESSONS: Although rare, nonsaccular type LDM may appear concurrently with intramedullary infantile hemangioma at the conus medullaris. The authors present a possible mechanism behind this concurrent presentation in the same area.
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spelling pubmed-105506772023-10-06 Limited dorsal myeloschisis associated with intramedullary infantile hemangioma in the conus medullaris: illustrative case Nakanishi, Yoko Kunihiro, Noritsugu Umaba, Ryoko Matsusaka, Yasuhiro Inoue, Takeshi Sakamoto, Hiroaki J Neurosurg Case Lessons Case Lesson BACKGROUND: Limited dorsal myeloschisis (LDM) and intramedullary infantile hemangioma rarely coexist in the spinal cord. OBSERVATIONS: The authors describe the case of a 3-month-old girl who, despite lacking neurological symptoms or signs, had a cigarette burn-like mark at the lumbosacral area and skin dimpling in the gluteal area. Magnetic resonance imaging showed a low-set conus due to a thickened filum and an abnormal subcutaneous stalk connected to the conus medullaris. In combination with the skin lesions, these findings strongly implied nonsaccular-type LDM. An intramedullary mass in the conus medullaris was also shown on magnetic resonance imaging and was homogenously enhanced with isointensity on T1- and T2-weighted images. We prophylactically untethered the spinal cord and partially removed the intramedullary mass, which had no clear borders, for a safe surgical dissection. Histologically, the intramedullary mass was an infantile hemangioma, and the subcutaneous stalk was a lesion associated with LDM. The patient remained neurologically intact after surgery, and then 2 years later, there was spontaneous regression of the residual tumor. LESSONS: Although rare, nonsaccular type LDM may appear concurrently with intramedullary infantile hemangioma at the conus medullaris. The authors present a possible mechanism behind this concurrent presentation in the same area. American Association of Neurological Surgeons 2023-04-24 /pmc/articles/PMC10550677/ /pubmed/37096816 http://dx.doi.org/10.3171/CASE22359 Text en © 2023 The authors https://creativecommons.org/licenses/by-nc-nd/4.0/CC BY-NC-ND 4.0 (http://creativecommons.org/licenses/by-nc-nd/4.0/ (https://creativecommons.org/licenses/by-nc-nd/4.0/) )
spellingShingle Case Lesson
Nakanishi, Yoko
Kunihiro, Noritsugu
Umaba, Ryoko
Matsusaka, Yasuhiro
Inoue, Takeshi
Sakamoto, Hiroaki
Limited dorsal myeloschisis associated with intramedullary infantile hemangioma in the conus medullaris: illustrative case
title Limited dorsal myeloschisis associated with intramedullary infantile hemangioma in the conus medullaris: illustrative case
title_full Limited dorsal myeloschisis associated with intramedullary infantile hemangioma in the conus medullaris: illustrative case
title_fullStr Limited dorsal myeloschisis associated with intramedullary infantile hemangioma in the conus medullaris: illustrative case
title_full_unstemmed Limited dorsal myeloschisis associated with intramedullary infantile hemangioma in the conus medullaris: illustrative case
title_short Limited dorsal myeloschisis associated with intramedullary infantile hemangioma in the conus medullaris: illustrative case
title_sort limited dorsal myeloschisis associated with intramedullary infantile hemangioma in the conus medullaris: illustrative case
topic Case Lesson
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10550677/
https://www.ncbi.nlm.nih.gov/pubmed/37096816
http://dx.doi.org/10.3171/CASE22359
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