A diffuse scalp neurofibroma in a 4-year-old child
- Authors: Kletskaya I.S.1, Serebrennikova P.A.1, Gassan T.A.1, Narbutov A.G.1, Makarova O.V.1
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Affiliations:
- N.I. Pirogov Russian National Research Medical University
- Issue: Vol 28, No 4 (2024)
- Pages: 384-391
- Section: CASE REPORTS
- Submitted: 03.08.2023
- Accepted: 08.07.2024
- Published: 09.09.2024
- URL: https://jps-nmp.ru/jour/article/view/706
- DOI: https://doi.org/10.17816/ps706
- ID: 706
Cite item
Abstract
BACKGROUND: Structures resembling Meissner's tactile corpuscles have been revealed in various peripheral nerve tumors, including schwannomas and neurofibromas, as well as in congenital melanocytic nevi and neural crest hamartomas. As a rule, Meissner's tactile corpuscles are few in number, but in rare cases they represent the predominant component of the formation tissue.
CLINICAL CASE DESCRIPTION: The authors describe a case of their observation: a 4 y.o. patient with diffuse neurofibroma consisting of structures resembling tactile corpuscles. Clinically, this fibroma looked like a defect in the occipital soft tissue region with excessive folding and alopecia. At the histological examination, the dermis and subcutaneous adipose tissue were seen involved in the pathological process. The formation tissue consisted mostly of "neuroid" structures resembling tactile corpuscles located among fibroblast-like cells with mast cell admixture in the infiltrate. An immunohistochemical examination revealed expression of S100 in them, EMA, GLUT1 in the perineuria, and CD34 in the stroma. Melanocytic marker (MelanA, HMB45) expression was not detected.
CONCLUSION: The case presented by the authors is of interest to professionals due to the rarity of this morphological variant, difficulties of clinical and histological differential diagnostics with other tumors and tumor-like processes in children.
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About the authors
Iryna S. Kletskaya
N.I. Pirogov Russian National Research Medical University
Author for correspondence.
Email: ikletskaya@gmail.com
ORCID iD: 0000-0002-8552-7682
SPIN-code: 1046-3870
MD
Россия, 117 Leninskiy avenue, 119571 MoscowPolina A. Serebrennikova
N.I. Pirogov Russian National Research Medical University
Email: blackbutlers@yandex.ru
ORCID iD: 0000-0002-9317-1671
SPIN-code: 7630-4720
MD
Россия, 117 Leninskiy avenue, 119571 MoscowTatiana A. Gassan
N.I. Pirogov Russian National Research Medical University
Email: tatgassan@mail.ru
ORCID iD: 0000-0001-7322-2892
MD, Dr. Sci. (Medicine), Professor
Россия, 117 Leninskiy avenue, 119571 MoscowAnton G. Narbutov
N.I. Pirogov Russian National Research Medical University
Email: anarbutov@mail.ru
ORCID iD: 0000-0003-0168-8671
MD, Cand. Sci. (Medicine)
Россия, 117 Leninskiy avenue, 119571 MoscowOlga V. Makarova
N.I. Pirogov Russian National Research Medical University
Email: makarovao77@mail.ru
ORCID iD: 0009-0002-7497-3502
MD
Россия, 117 Leninskiy avenue, 119571 MoscowReferences
- Elder D, Massi D, Scolyer R, Willemze R. WHO classification of skin tumours, 4th edition. WHO Press; 2018.
- Watabe K. Immunohistochemical and ultrastructural studies on tactile-like corpuscles in neurofibromas. No To Shinkei. 1985;37(8):799–807. (In Japan)
- Sode T, Kunzler E, Uzoma B, et al. A meissnerian neurofibroma: Case report of a rare neurofibroma variant. J Cutan Pathol. 2020;47(10):967–969. doi: 10.1111/cup.13759
- Hill RP. Neuroma of Wagner-Meissner tactile corpuscles. Cancer. 1951;4(4):879–882. doi: 10.1002/1097-0142(195107)4:4<879::aid-cncr2820040425>3.0.co;2-2
- Kaiserling E, Geerts ML. Tumour of Wagner-Meissner touch corpuscles. Wagner-Meissner neurilemmoma. Virchows Arch A Pathol Anat Histopathol. 1986;409(2):241–250. doi: 10.1007/BF00708331
- Smith KJ, Mezebish D, Williams J, et al. The spectrum of neurocristic cutaneous hamartoma: Clinicopathologic and immunohistochemical study of three cases. Ann Diagn Pathol. 1998;2(4):213–223. doi: 10.1016/s1092-9134(98)80010-5
- Stieler KM, Rowert-Huber J, Vogt A, et al. Cutaneous cephalic neurocristic hamartoma on the head with melanocytic, cartilage, blood vessel, neural, and bony tissue. Am J Dermatopathol. 2021;43(4):284–286. doi: 10.1097/DAD.0000000000001826
- Karamitopoulou-Diamantis E, Paredes B, Vajtai I. Cutaneous neurocristic hamartoma with blue naevus-like features and plexiform dermal hyperneury. Histopathology. 2006;49(3):326–328. doi: 10.1111/j.1365-2559.2006.02459.x
- Turel MK, Chacko G, Raja A, Scheithauer BW. Neurocristic cutaneous hamartoma of the scalp. J Pediatr Neurosci. 2012;7(3): 181–184. doi: 10.4103/1817-1745.106473
- Wong J, Roy SF, Kokta V. Neurocristic cutaneous hamartoma with perineuriomatous differentiation: Can it be distinguished from perineuriomatous melanocytic nevi? Am J Dermatopathol. 2021;43(10):757–758. doi: 10.1097/DAD.0000000000001934