Abstract
Background
Perineural spread (PNS) is an emerging mechanism for progressive, non-traumatic brachial plexopathy. We aim to summarize the pathologies (tumor and infection) shown to have spread along or to the brachial plexus, and identify the proposed mechanisms of perineural spread.
Methods
A focused review of the literature was performed pertaining to pathologies with identified perineural spread to the brachial plexus.
Results
We summarized pathologies currently reported to have PNS in the brachial plexus and offer a structure for understanding and describing these pathologies with respect to their interaction with the peripheral nervous system.
Conclusions
Perineural spread is an underrepresented entity in the literature, especially regarding the brachial plexus. It can occur via a primary or secondary mechanism based on the anatomy, and understanding this mechanism helps to support biopsies of sacrificial nerve contributions, leading to more effective and timely treatment plans for patients.
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References
Alsarraf LA, Shah KB, Hessel AC, Williams MD, Ginsberg LE (2016) Perineural spread along the intermediate branch of the supraclavicular nerve: a case report. Neurographics 6:16–19. https://doi.org/10.3174/ng.1160138
Balink H, de Visscher JG, van der Meij EH (2014) Recurrent head and neck desmoplastic melanoma with perineural spread along the nervus mandibularis revealed by 18F-FDG PET/CT. Int J Oral Maxillofac Surg 43:941–943. https://doi.org/10.1016/j.ijom.2014.04.004
Bansal M, Martin SR, Rudnicki SA, Hiatt KM, Mireles-Cabodevila E (2011) A rapidly progressing Pancoast syndrome due to pulmonary mucormycosis: a case report. J Med Case Rep 5:388. https://doi.org/10.1186/1752-1947-5-388
Barnett SL, Wells MJ, Mickey B, Hatanpaa KJ (2011) Perineural extension of cutaneous desmoplastic melanoma mimicking an intracranial malignant peripheral nerve sheath tumor. Case report. J Neurosurg 115:273–277. https://doi.org/10.3171/2011.4.JNS10913
Behnke NK, Crosby SN, Stutz CM, Holt GE (2013) Periscapular amputation as treatment for brachial plexopathy secondary to recurrent breast carcinoma: a case series and review of the literature. Eur J Surg Oncol 39:1325–1331. https://doi.org/10.1016/j.ejso.2013.10.005
Binder DK, Smith JS, Barbaro NM (2004) Primary brachial plexus tumors: imaging, surgical, and pathological findings in 25 patients. Neurosurg Focus 16:E11. https://doi.org/10.3171/foc.2004.16.5.12
Bourque PR, Warman Chardon J, Bryanton M, Toupin M, Burns BF, Torres C (2018) Neurolymphomatosis of the brachial plexus and its branches: case series and literature review. Can J Neurol Sci 45:137–143. https://doi.org/10.1017/cjn.2017.282
Briani C, Visentin A, Campagnolo M, Salvalaggio A, Ferrari S, Cavallaro T, Manara R, Gasparotti R, Piazza F (2019) Peripheral nervous system involvement in lymphomas. J Peripher Nerv Syst 24:5–18. https://doi.org/10.1111/jns.12295
Calabek B, Meng S, Pollanz S, Klepetko W, Hoetzenecker K, Oberndorfer F, Grisold W (2015) A case of Pancoast tumor with unusual presentation. J Brachial Plex Peripher Nerve Inj 10:e53–e56. https://doi.org/10.1055/s-0035-1551654
Capek S, Amrami KK, Howe BM, Salomao DR, Dyck PJ, Spinner RJ (2015) Perineural spread of squamous cell carcinoma: from skin to skin through the brachial plexus. Clin Neurol Neurosurg 128:90–93. https://doi.org/10.1016/j.clineuro.2014.11.004
Capek S, Amrami KK, Spinner RJ (2016) Gastroesophageal junction carcinoma and brachial plexopathy: An anatomic explanation via perineural spread. Clin Anat 29:800–803. https://doi.org/10.1002/ca.22708
Chan YJ, Chen SL (2009) Nerve invasion by epithelial cells in benign breast diseases. J Chin Med Assoc 72:150–152. https://doi.org/10.1016/S1726-4901(09)70041-3
Chang PC, Fischbein NJ, McCalmont TH, Kashani-Sabet M, Zettersten EM, Liu AY, Weissman JL (2004) Perineural spread of malignant melanoma of the head and neck: clinical and imaging features. AJNR Am J Neuroradiol 25:5–11
Choi JY, Kang CH, Kim BJ, Park KW, Yu SW (2009) Brachial plexopathy following herpes zoster infection: two cases with MRI findings. J Neurol Sci 285:224–226. https://doi.org/10.1016/j.jns.2009.05.016
Cooper D (1974) Malignant mesothelioma invading the spinal canal. Postgrad Med J 50:718–723. https://doi.org/10.1136/pgmj.50.589.718
Dastur DK (1983) Pathology and pathogenesis of predilective sites of nerve damage in leprous neuritis. Nerves in the arm and the face. Neurosurg Rev 6:139–152. https://doi.org/10.1007/bf01742765
Davis GA, Knight S (2007) Pancoast tumor resection with preservation of brachial plexus and hand function. Neurosurg Focus 22:E15
Duraker N, Caynak ZC, Turkoz K (2006) Perineural invasion has no prognostic value in patients with invasive breast carcinoma. Breast 15:629–634. https://doi.org/10.1016/j.breast.2005.12.003
El-Barrany WG, Marei AG, Vallee B (1999) Anatomic basis of vascularised nerve grafts: the blood supply of peripheral nerves. Surg Radiol Anat 21:95–102. https://doi.org/10.1007/s00276-999-0095-9
Expert Panel on Neurologic I, Bykowski J, Aulino JM, Berger KL, Cassidy RC, Choudhri AF, Kendi AT, CFE K, Luttrull MD, Sharma A, Shetty VS, Than K, Winfree CJ, Cornelius RS (2017) ACR Appropriateness Criteria((R)) Plexopathy. J Am Coll Radiol 14:S225–S233. https://doi.org/10.1016/j.jacr.2017.02.002
Fabian VA, Wood B, Crowley P, Kakulas BA (1997) Herpes zoster brachial plexus neuritis. Clin Neuropathol 16:61–64
Ferner RE, Gutmann DH (2002) International consensus statement on malignant peripheral nerve sheath tumors in neurofibromatosis. Cancer Res 62:1573–1577
Frey I, Le Breton C, Lefkopoulos A, Perrot N, Khalil A, Chopier J, Le Blanche A, Bigot JM (1998) Intradural extramedullary spinal canal secondary neoplasms: MR findings in 30 patients. Eur Radiol 8:1187–1192. https://doi.org/10.1007/s003300050532
Frydenlund N, Leone DA, Mitchell B, Yang S, Deng A, Hoang MP, Mahalingam M (2015) Neurotrophin receptors and perineural invasion in desmoplastic melanoma. J Am Acad Dermatol 72:851–858. https://doi.org/10.1016/j.jaad.2015.01.026
Ghia D, Gadkari R, Nayak C (2012) Complex regional pain syndrome secondary to leprosy. Pain Med 13:1067–1071. https://doi.org/10.1111/j.1526-4637.2012.01426.x
Gilder HE, Puffer RC, Bydon M, Spinner RJ (2018) The implications of intradural extension in paraspinal malignant peripheral nerve sheath tumors: effects on central nervous system metastases and overall survival. J Neurosurg Spine 29:725–728. https://doi.org/10.3171/2018.5.SPINE18445
Gwathmey KG (2018) Plexus and peripheral nerve metastasis. Handb Clin Neurol 149:257–279. https://doi.org/10.1016/B978-0-12-811161-1.00017-7
Hebert-Blouin MN, Amrami KK, Loukas M, Spinner RJ (2011) A proposed anatomical explanation for perineural spread of breast adenocarcinoma to the brachial plexus. Clin Anat 24:101–105. https://doi.org/10.1002/ca.21079
Ismail A, Rao DG, Sharrack B (2009) Pure motor Herpes Zoster induced brachial plexopathy. J Neurol 256:1343–1345. https://doi.org/10.1007/s00415-009-5149-8
Iwamoto S, Odland PB, Piepkorn M, Bothwell M (1996) Evidence that the p75 neurotrophin receptor mediates perineural spread of desmoplastic melanoma. J Am Acad Dermatol 35:725–731. https://doi.org/10.1016/s0190-9622(96)90728-8
Jack AS, Shah V, Ramey WL, Bowman C, Huie CJ, Jacques LG (2020) Brachial plexus mucormycosis secondary to perineurial spread: literature review and case report of a rare mode of infectious spread. Interdiscip Neurosurg 20. https://doi.org/10.1016/j.inat.2020.100687
James AW, Shurell E, Singh A, Dry SM, Eilber FC (2016) Malignant peripheral nerve sheath tumor. Surg Oncol Clin N Am 25:789–802. https://doi.org/10.1016/j.soc.2016.05.009
Jayakumar N, Ismail H, Athar S, Ashwood N (2020) Perineural invasion in intramedullary spinal cord metastasis. Ann R Coll Surg Engl:e1–e3. https://doi.org/10.1308/rcsann.2020.0009
Jones LK Jr, Reda H, Watson JC (2014) Clinical, electrophysiologic, and imaging features of zoster-associated limb paresis. Muscle Nerve 50:177–185. https://doi.org/10.1002/mus.24141
Kalfas F, Scudieri C (2020) Intramedullary metastasis to the cervical spinal cord from malignant pleural mesothelioma: review of the literature and case reports. Asian J Neurosurg 15:70–75. https://doi.org/10.4103/ajns.AJNS_234_18
Karak SG, Quatrano N, Buckley J, Ricci A Jr (2010) Prevalence and significance of perineural invasion in invasive breast carcinoma. Conn Med 74:17–21
Kim JG, Chung SG (2016) Herpetic brachial plexopathy: application of brachial plexus magnetic resonance imaging and ultrasound-guided corticosteroid injection. Am J Phys Med Rehabil 95:e67–e71. https://doi.org/10.1097/PHM.0000000000000445
Kim DH, Murovic JA, Tiel RL, Moes G, Kline DG (2005) A series of 397 peripheral neural sheath tumors: 30-year experience at Louisiana State University Health Sciences Center. J Neurosurg 102:246–255. https://doi.org/10.3171/jns.2005.102.2.0246
Kim J, Jeon JY, Choi YJ, Choi JK, Kim SB, Jung KH, Ahn JH, Kim JE, Seo S (2020) Characteristics of metastatic brachial plexopathy in patients with breast cancer. Support Care Cancer 28:1913–1918. https://doi.org/10.1007/s00520-019-04997-6
Kolokythas A, Cox DP, Dekker N, Schmidt BL (2010) Nerve growth factor and tyrosine kinase A receptor in oral squamous cell carcinoma: is there an association with perineural invasion? J Oral Maxillofac Surg 68:1290–1295. https://doi.org/10.1016/j.joms.2010.01.006
Kotoulas C, Psathakis K, Tsintiris K, Sampaziotis D, Karnesis L, Laoutidis G (2006) Pulmonary mucormycosis presenting as Horner’s syndrome. Asian Cardiovasc Thorac Ann 14:86–87. https://doi.org/10.1177/021849230601400123
Lederman RJ, Wilbourn AJ (1984) Brachial plexopathy: recurrent cancer or radiation? Neurology 34:1331–1335. https://doi.org/10.1212/wnl.34.10.1331
Levy H, Sacho H, Feldman C, Naude GE, Peskin J, Stead KJ, Kallenbach JM (1986) Pulmonary mucormycosis presenting with Horner’s syndrome. Report of a medical cure. S Afr Med J 70:363–365
Marek T, Howe BM, Amrami KK, Spinner RJ (2018) Perineural spread of nonmelanoma skin cancer to the brachial plexus: identifying anatomic pathway(s). World Neurosurg 114:e818–e823. https://doi.org/10.1016/j.wneu.2018.03.092
Marek T, Laughlin RS, Howe BM, Spinner RJ (2018) Perineural spread of melanoma to the brachial plexus: identifying the anatomic pathway(s). World Neurosurg 111:e921–e926. https://doi.org/10.1016/j.wneu.2018.01.031
Mizuma A, Kijima C, Nagata E, Takizawa S (2016) A case of suspected breast cancer metastasis to brachial plexus detected by magnetic resonance neurography. Case Rep Oncol 9:395–399. https://doi.org/10.1159/000447054
Nalini A, Singh RJ, Saini J, Prasad C, Mahadevan A (2015) Magnetic resonance neurography identifies involvement of plexuses in leprous neuropathy. Neurol India 63:624–626. https://doi.org/10.4103/0028-3886.162102
Newlin HE, Morris CG, Amdur RJ, Mendenhall WM (2005) Neurotropic melanoma of the head and neck with clinical perineural invasion. Am J Clin Oncol 28:399–402. https://doi.org/10.1097/01.coc.0000144853.76112.3d
Omar AT 2nd, Villaruel AR, Khu KJO (2020) Tuberculoma of the peripheral nerve: illustrative case and systematic review of the literature. World Neurosurg 137:e547–e553. https://doi.org/10.1016/j.wneu.2020.02.031
Omar AT 2nd, Villaruel AR, Khu KJO (2020) Tuberculoma of the peripheral nerve: illustrative case and systematic review of the literature. World Neurosurg. https://doi.org/10.1016/j.wneu.2020.02.031
Panagopoulos N, Leivaditis V, Koletsis E, Prokakis C, Alexopoulos P, Baltayiannis N, Hatzimichalis A, Tsakiridis K, Zarogoulidis P, Zarogoulidis K, Katsikogiannis N, Kougioumtzi I, Machairiotis N, Tsiouda T, Kesisis G, Siminelakis S, Madesis A, Dougenis D (2014) Pancoast tumors: characteristics and preoperative assessment. J Thorac Dis 6(Suppl 1):S108–S115. https://doi.org/10.3978/j.issn.2072-1439.2013.12.29
Paraf F, Flejou JF, Pignon JP, Fekete F, Potet F (1995) Surgical pathology of adenocarcinoma arising in Barrett’s esophagus. Analysis of 67 cases. Am J Surg Pathol 19:183–191. https://doi.org/10.1097/00000478-199502000-00007
Payne R, Baccon J, Dossett J, Scollard D, Byler D, Patel A, Harbaugh K (2015) Pure neuritic leprosy presenting as ulnar nerve neuropathy: a case report of electrodiagnostic, radiographic, and histopathological findings. J Neurosurg 123:1238–1243. https://doi.org/10.3171/2014.9.JNS142210
Puffer RC, Marek T, Stone JJ, Raghunathan A, Howe BM, Spinner RJ (2018) Extensive perineural spread of an intrapelvic sciatic malignant peripheral nerve sheath tumor: a case report. Acta Neurochir 160:1833–1836. https://doi.org/10.1007/s00701-018-3619-4
Restrepo CE, Spinner RJ, Howe BM, Jentoft ME, Markovic SN, Lachance DH (2015) Perineural spread of malignant melanoma from the mandible to the brachial plexus: case report. J Neurosurg 122:784–790. https://doi.org/10.3171/2014.12.JNS14852
Roh J, Muelleman T, Tawfik O, Thomas SM (2015) Perineural growth in head and neck squamous cell carcinoma: a review. Oral Oncol 51:16–23. https://doi.org/10.1016/j.oraloncology.2014.10.004
Shamji FM, Leduc JR, Bormanis J, Sachs HJ (1988) Acute Pancoast’s syndrome caused by fungal infection. Can J Surg 31:441–443
Shibuya K, Misawa S, Hirano S, Kuwabara S (2013) Acute brachial plexopathy caused by Burkitt’s lymphoma infiltration. Intern Med 52:931. https://doi.org/10.2169/internalmedicine.52.9156
Song M, Sun X, Sun R, Liu T, Li G, Liu S, Lu M, Qu W (2016) Ulnar nerve tuberculoma: a case report and literature review. J Clin Neurosci 32:130–133. https://doi.org/10.1016/j.jocn.2015.12.047
Stark AM, Mehdorn HM (2013) Leptomeningeal metastasis of an intradural malignant peripheral nerve sheath tumor. J Clin Neurosci 20:1181–1183. https://doi.org/10.1016/j.jocn.2012.09.039
Stark AM, Buhl R, Hugo HH, Mehdorn HM (2001) Malignant peripheral nerve sheath tumours--report of 8 cases and review of the literature. Acta Neurochir 143:357–363; discussion 363-354. https://doi.org/10.1007/s007010170090
Stubblefield MD (2017) Neuromuscular complications of radiation therapy. Muscle Nerve 56:1031–1040. https://doi.org/10.1002/mus.25778
Visser LH, Jain S, Lokesh B, Suneetha S, Subbanna J (2012) Morphological changes of the epineurium in leprosy: a new finding detected by high-resolution sonography. Muscle Nerve 46:38–41. https://doi.org/10.1002/mus.23269
Warwar RE, Bullock JD (1998) Rhino-orbital-cerebral mucormycosis: a review. Orbit 17:237–245. https://doi.org/10.1076/orbi.17.4.237.2742
White HD, White BA, Boethel C, Arroliga AC (2011) Pancoast’s syndrome secondary to infectious etiologies: a not so uncommon occurrence. Am J Med Sci 341:333–336. https://doi.org/10.1097/MAJ.0b013e3181fa2e2d
Laothamatas J, Hemachudha T, Mitrabhakdi E, Wannakrairot P, Tulayadaechanont S (2003) MR imaging in human rabies. AJNR Am J Neuroradiol 24:1102–1109
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Murthy, N.K., Amrami, K.K. & Spinner, R.J. Perineural spread to the brachial plexus: a focused review of proposed mechanisms and described pathologies. Acta Neurochir 162, 3179–3187 (2020). https://doi.org/10.1007/s00701-020-04466-8
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DOI: https://doi.org/10.1007/s00701-020-04466-8