Spinal meningeal melanocytoma in a 5-year-old child: a case report and review of literature
Meningeal melanocytoma is considered a rare lesion arising from leptomeningeal melanocytes. Nearly two thirds of meningeal melanocytomas were reported in the intracranial compartment and the remaining one third in the spine. Spinal melanocytomas can be extradural or intradural, with extradural variant being more common, and the majority of cases have been single reports.
A 5-year-old male presented with a 4-month history of non-radiating low back pain persistent at rest, with otherwise non-remarkable medical history. The patient was neurologically intact with no deficits. Preoperatively, routine laboratory investigations were non-remarkable. MRI imaging was done and showed a lesion at the level of T11 to L4, hyperintense on T1 and hypointense on T2 with homogenous contrast enhancement. Intraoperatively, the lesion was hemorrhagic, brownish, and rubbery in consistency attached to the ventral dura. Microscopic picture revealed dense cytoplasmic brown melanin pigments, with no significant mitoses or nuclear atypia. What is unique about our case is the age of the patient (5 years).
To the best of our knowledge, after reviewing the literature, this is the youngest case to be reported.
SMM is an extremely rare tumor with a benign course. Complete surgical excision should be attempted. Age of presentation may be as young as in our case and the diagnosis of such a tumor should never be excluded in this early age group with persistent low back ache.
KeywordsMelanocytoma Meningeal Spinal tumors Pediatric Melanoma
Epithelial membrane antigen
Spinal meningeal melanocytoma
Meningeal melanocytoma is considered a rare lesion arising from leptomeningeal melanocytes. It is the benign pole of the spectrum of neoplastic leptomeningeal melanocyte proliferations that involves primary malignant melanoma at the other pole, from which it differs in behavior and aggressiveness by owing a much better prognosis than its malignant variant (Painter et al. 2000). They may arise anywhere in the cranial and spinal meninges. Two thirds of meningeal melanocytomas were reported in the intracranial compartment and the remaining one third in the spine (Wang et al. 2013). Though rare, local recurrence or leptomeningeal spread secondary to malignant transformation has been reported years after the initial diagnosis (Wang et al. 2007). Spinal melanocytomas can be extradural or intradural, with extradural variant being more common. With around 60 cases reported in the literature, the majority of cases have been single reports (Mangels et al. 2006). We present this case being the youngest patient diagnosed with spinal meningeal melanocytoma. Written informed consent was obtained from the patient for publication of this case report and accompanying images.
Discussion and evaluation
Melanocytoma is a pigmented neoplasm of the meninges, which arises from melanocytes derived from the neural crest (Turhan et al. 2004). It is a rare tumor and was first described in 1972 by Limas and Tio (1972). It usually occurs in the spine and posterior fossa (Shanthi et al. 2010). What is unique about our case is the age of the patient (5 years). To the best of our knowledge after reviewing the literature, this is the youngest case to be reported (Clarke et al. 1998). The usual age of presentation is usually around the fifth decade (Czarnecki et al. 1997; Hou et al. 2012), with age ranging from 9 to 79 years in different case reports reviewed (Shanthi et al. 2010; Clarke et al. 1998; Czarnecki et al. 1997; Hou et al. 2012; Alameda et al. 1998). In the study of Yang et al. (2016) (the largest case series in literature) which included 15 patients from the period of 2004–2014, the youngest patient was 14 years. The youngest case reported before our case was 9 years in the study of Alameda F. et al. in 1998 (Alameda et al. 1998).
As for clinical presentation, our case had only a 4-month history of non-radiating low back pain with no radiculopathy or sphincter affection. In literature, the most common feature was radiculopathy, either pain or heaviness followed by back pain and sphincter affection (Czarnecki et al. 1997; Hou et al. 2012; Yang et al. 2016; Dorwal et al. 2014; Sen et al. 2011).
For spinal meningeal melanocytoma (SMM), it is usually intradural extramedullary and to a lesser extent intramedullary (Of all 60 SMM, 40 cases were intradural extramedullary and 19 cases were intramedullary.) and this goes along with our case, with cervical levels being affected more than dorsal levels, and the lumbar levels were the least (Clarke et al. 1998; Hou et al. 2012; Alameda et al. 1998; Eun et al. 2011).
As for the radiological appearance, it correlates well with the available literature (Hou et al. 2012; Alameda et al. 1998). The signal intensity in different sequences depends mainly on the concentration of the melanin pigment in the tumor and so does the contrast enhancement. Lesions with high melanin content may show subtle contrast enhancement on T1WI with contrast as it may be masked by the hyperintensity of melanin (Alameda et al. 1998).
Surgical resection is the main choice for treatment of SMMs. These are benign lesion which can be excised totally whether being intradural extramedullary (possibly en bloc) or intramedullary lesions (Yang et al. 2016; Horn et al. 2008). Our lesion was subtotally resected due to the intermingled part with the conus medullaris. Local control by radiotherapy is advisable in case of incomplete excision, as recurrence may transform into malignant melanoma (Rades et al. 2004). Even in complete resection, some authors recommend radiotherapy, as recurrence was reported in 22% of cases at 5 years (Rades and Schild 2006). However, we decided not to administer radiotherapy and to follow the lesion with serial imaging studies, owing to the benign nature of the lesion and the young age of the patient who could be harmed by the potential adverse effects of radiotherapy on a young age. Stereotactic radiosurgery is another acceptable alternative with a favorable outcome after incomplete resection (Ali et al. 2009).
SMM is an extremely rare tumor with a benign course. Surgical excision in an en bloc manner should be the model. The outcome is generally good with complete remission and long-term free survival. Age of presentation may be as young as in our case and the diagnosis of such a tumor should never be excluded in this early age group with persistent low back pain.
AS carried out the literature search and review. HA carried out the manuscript preparation. MA performed the manuscript editing. AK carried out the immunohistochemistry studies and helped to draft the manuscript. AA collected the clinical and surgical data. All authors read and approved the final manuscript.
Ethics approval and consent to participate
Consent for publication
Written informed consent was obtained from the patient for publication of this case report and accompanying images.
The authors declare that they have no competing interests.
Springer Nature remains neutral with regard to jurisdictional claims in published maps and institutional affiliations.
- Eun SS, Kim HS, Lee SH, Liu WC, Lee JH. Spinal meningeal melanocytoma in the S-1 nerve root sheath with paraspinal extension mimicking schwannoma. World Neurosurg. 2011;75(2):303–6. Available from: https://doi.org/10.1016/j.wneu.2010.06.034. Elsevier Inc
- Sen R, Sethi D, Goyal V, Duhan A, Modi S. Spinal meningeal melanocytoma. Asian J Neurosurg. 2011;6(2):110–2.Google Scholar
- Shanthi V, Ramakrishna BA, Bheemaraju VV, Rao NM, Athota VRM. Spinal meningeal melanocytoma: a rare meningeal tumor. Ann Indian Acad Neurol. 2010;13(4):308–10. Available from: http://www.ncbi.nlm.nih.gov/pmc/articles/PMC3021939/.CrossRefPubMedPubMedCentralGoogle Scholar
Open AccessThis article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made.