scholarly journals Collision tumors in the spinal cord: Co-existent intramedullary dermoid with spinal lipoma

2020 ◽  
Vol 21 ◽  
pp. 100751
Author(s):  
Jaskaran Singh Gosal ◽  
Kartikeya Shukla ◽  
Mayank Garg ◽  
Suryanarayanan Bhaskar ◽  
Deepak Kumar Jha
Neurosurgery ◽  
1986 ◽  
Vol 18 (5) ◽  
pp. 611-615 ◽  
Author(s):  
David G. McLone ◽  
Thomas P. Naidich

Abstract The value of laser resection was assessed in the last 50 of 128 consecutive cases of pediatric spinal lipoma. In this series, there was no mortality. No patient suffered increase in neurological or urological deficit. Postoperatively, 8 of 20 patients with prior motor deficit (40%) had substantially improved motor function. Two of 17 previously incontinent patients became continent of urine (12%). Use of the CO2 laser reduced the length of operation, the intraoperative blood loss, and the degree of manipulation of the spinal cord and nerve roots. Most of the fat could be removed successfully from the liponeural junction, permitting more nearly anatomical removal of the intramedullary component of the lesion and greater ease in replacing the cord into a reconstructed arachnoid-dural canal. In the authors' opinions, proper management of the patient with spinal lipoma now requires early prophylactic resection of the lipoma and untethering of the spinal cord.


2016 ◽  
Vol 2 (1) ◽  
Author(s):  
Andreas Ficklscherer ◽  
Anja Ziwen Zhang ◽  
Andrea Baur-Melnyk ◽  
Thomas Knösel ◽  
Volkmar Jansson ◽  
...  

1971 ◽  
Vol 35 (3) ◽  
pp. 335-337 ◽  
Author(s):  
Renato Giuffrè ◽  
Domenico Gambacorta

✓ A case of intradural spinal lipoma has been reported. Its pathological and clinical features are compared with those of 129 other cases collected from the literature.


Author(s):  
Yumiko Komori ◽  
Masahiro Nonaka ◽  
Takamasa Kamei ◽  
Junichi Takeda ◽  
Tetsuo Hashiba ◽  
...  

The authors present the case of a 1-month-old girl with a lumbosacral lipoma who then developed an extracanalicular syrinx and experienced rapid deterioration. The patient’s initial MRI study, obtained before she became symptomatic, revealed a spinal lipoma with a syrinx in contact with the lipoma-cord interface. She was initially asymptomatic but developed loss of motor function in the left leg 14 days after MRI. Emergency surgery was performed. Intraoperative findings revealed a swollen spinal cord. Lipomatous tissue on the caudal side of the conus was removed subtotally, and the central canal was opened. Expansion of the syrinx was observed intraoperatively. Postoperatively, the patient’s left leg paresis remained. Postoperative MRI revealed rostral and extracanalicular expansion of the syrinx. This is the first report on the rapid deterioration of a conus lipoma due to extracanalicular expansion of a syrinx. Careful follow-up and repeat MRI should be considered for patients with spinal lipomas with syringomyelia, especially when the syrinx is attached to the lipoma-cord interface.


2021 ◽  
Vol 12 ◽  
pp. 633
Author(s):  
Kiyoharu Shimizu ◽  
Takafumi Mitsuhara ◽  
Masaaki Takeda ◽  
Satoshi Yamaguchi

Background: The evolution of syrinx formation has rarely been documented. Here, we report a patient whose “presyrinx” evolved on successive magnetic resonance (MR) images to a mature syrinx. Case Description: A patient had a lipoma and tethered cord at birth. At 3 weeks of age, he had undergone a partial removal of the lipoma and untethering of the spinal cord. At age 6, the thoracic MR images showed edema within the gray matter of the cord at the T7 level, consistent with a “presyrinx.” In addition, subsequent MR studies (i.e., at age 7) showed a small cavity in the right posterior horn of the cord accompanied by further expansion throughout the right-sided gray matter. Despite repeated cord untethering at age 7, the T7 parenchymal cord change evolved into a mature syrinx by age 10. Conclusion: An infant with a lipoma/tethered cord, despite two instances of cord detethering (i.e., ages 3 weeks and 7 years), showed continued MR evolution of a “presyrinx” to a mature syrinx by age 10.


2021 ◽  
Vol 1 (3) ◽  
Author(s):  
Matthew T. Neal ◽  
Alexandra E. Richards ◽  
Kara L. Curley ◽  
Kliment Donev ◽  
Mark K. Lyons ◽  
...  

BACKGROUNDIntramedullary spinal cord tumors represent a minority of intradural tumors. Among intramedullary spinal cord tumors, hemangioblastomas are uncommon, and schwannomas are extremely rare. Collision tumors are histologically distinct tumors that are intermingled and growing together.OBSERVATIONSIn this report, the authors describe a patient with a cervical intramedullary collision tumor involving a hemangioblastoma and schwannoma. To the authors’ knowledge, no prior spinal intramedullary collision tumor involving multiple neoplasms has been described. The patient’s presentation and management are described.LESSONSClinicians should consider the possibility of collision tumors when evaluating intramedullary spinal cord tumors, especially when patient presentation and radiographic findings are atypical. When tumors with similar radiographic characteristics form collision tumors, distinction using preoperative imaging can be extremely challenging. In addition, surgical management of intramedullary collision tumors, like that for all intramedullary spinal cord tumors, should involve meticulous perioperative care and a methodical surgical technique. Maximal safe resection will depend upon histopathological diagnosis, anatomical location of the tumor, presence of distinct dissection planes, and stability of neuromonitoring. Finally, ongoing research on the genetics of intramedullary spinal cord tumors may identify underlying genetic links for intramedullary hemangioblastomas and schwannomas.


2021 ◽  
Vol 8 (8) ◽  
Author(s):  
Antonio GL Jr ◽  
◽  
Abreu NMP ◽  
Leal MVB ◽  
Rodrigues JPC ◽  
...  

Lipoma is a rare and benign tumor, with lesions associated with spinal dysraphisms. The reported case is about an 8-month-old child who arrived at the hospital with developmental delay, excessive crying, undergoing MRI and reported spinal cord lipoma. Intradural lipomas without association with dysraphism are difficult to diagnose, being the most accurate form of MRI.


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