Characteristics, Natural Course and Treatment of Intramuscular Capillary-type Haemangioma: A Systematic Literature Review

Authors

  • Jordan Orly CHRU Tours, Department of Dermatology, Unit of Pediatric dermatology, Tours, France; Reference center for genodermatoses and rare skin diseases (MAGEC-Tours), Tours https://orcid.org/0000-0002-6463-3187
  • Annouk Bisdorff 3Reference center for vascular anomalies FAVA-multi, University Hospital of Lariboisière; Coordinator of the constitutive center for superficial arteriovenous malformations in children and adults; AP-HP, Department of Neuroradiology, Paris, France
  • Aline Joly Reference center for genodermatoses and rare skin diseases (MAGEC-Tours), Tours, France; Reference center for vascular anomalies FAVA-multi, University Hospital of Lariboisière; Coordinator of the constitutive center for superficial arteriovenous malformations in children and adults; AP-HP, Department of Neuroradiology, Paris, France; CHRU Tours, Department of Maxillo-facial surgery, Tours, France
  • Afi-Emiliène Edee Reference center for genodermatoses and rare skin diseases (MAGEC-Tours), Tours, France
  • Elsa Tavernier University of Tours, University of Nantes, INSERM 1246-SPHERE, Tours, France; CHRU Tours, Clinical Investigation Center INSERM 1415, Tours, France
  • Denis Herbreteau Department of Neuroradiology, CHRU Tours, Tours, France https://orcid.org/0000-0002-4533-4296
  • Olivia Boccara Department of Dermatology and Reference center for genodermatoses and rare skin diseases (MAGEC-Necker), University Hospital Necker-Enfants Malades, Paris, France https://orcid.org/0000-0003-3508-2539
  • Michel Wassef Department of Pathology, University Hospital of Lariboisière, AP-HP, Paris, France https://orcid.org/0000-0001-9768-9788
  • Annabel Maruani CHRU Tours, Department of Dermatology, Unit of Pediatric dermatology, Tours, France; Reference center for genodermatoses and rare skin diseases (MAGEC-Tours), Tours, France; University of Tours, University of Nantes, INSERM 1246-SPHERE, Tours, France https://orcid.org/0000-0003-3734-810X

DOI:

https://doi.org/10.2340/actadv.v103.4432

Keywords:

Intra-muscular hemangioma, Intramuscular capillary-type hemangioma, Fast-flow, Intramuscular vascular malformation, Extracranial arteriovenous malformation, Intramuscular fast-flow vascular anomaly

Abstract

Intramuscular capillary-type haemangiomas (ICTH) are rare vascular anomalies that can easily be misdiagnosed as other entities. A systematic review was performed of all cases of ICTH in the literature since its first description in 1972. An adjudication committee reviewed cases to include only ICTHs. Among 1,143 reports screened, 43 were included, involving 75 patients. The most frequent differential diagnosis was intramuscular venous malformations. The mean age of patients at diagnosis was 21.2 years. ICTH was mainly described as a gradually increasing mass (81.8%), painless (73.9%), that could occur anywhere in the body but most frequently on the head and neck (44.0%). Magnetic resonance imaging (MRI) was mainly used for diagnosis (69.1%) and displayed specific features. The most frequent treatment was complete surgical removal (73.9%), which could be preceded by embolization, and led to complete remission without recurrence in all but 1 case.

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References

Allen PW, Enzinger FM. Hemangioma of skeletal muscle. An analysis of 89 cases. Cancer 1972; 29: 8-22.

https://doi.org/10.1002/1097-0142(197201)29:1<8::AID-CNCR2820290103>3.0.CO;2-A DOI: https://doi.org/10.1002/1097-0142(197201)29:1<8::AID-CNCR2820290103>3.0.CO;2-A

Yilmaz S, Kozakewich HP, Alomari AI, Fishman SJ, Mulliken JB, Chaudry G. Intramuscular capillary-type hemangioma: radiologic-pathologic correlation. Pediatr Radiol 2014; 44: 558-565.

https://doi.org/10.1007/s00247-014-2876-5 DOI: https://doi.org/10.1007/s00247-014-2876-5

Griffin N, Khan N, Thomas JM, Fisher C, Moskovic EC. The radiological manifestations of intramuscular haemangiomas in adults: magnetic resonance imaging, computed tomography and ultrasound appearances. Skeletal Radiol 2007; 36: 1051-1059.

https://doi.org/10.1007/s00256-007-0375-6 DOI: https://doi.org/10.1007/s00256-007-0375-6

Beham A, Fletcher CD. Intramuscular angioma: a clinicopathological analysis of 74 cases. Histopathology 1991; 18: 53-59.

https://doi.org/10.1111/j.1365-2559.1991.tb00814.x DOI: https://doi.org/10.1111/j.1365-2559.1991.tb00814.x

DeGiovanni JC, Simmonds J, Lang-Orsini M, Lee A. Recurrent intramuscular hemangioma (infiltrating angiolipoma) of the lower lip: a case report and review of the literature. Ear Nose Throat J 2022; 101: 306-311.

https://doi.org/10.1177/0145561320957759 DOI: https://doi.org/10.1177/0145561320957759

Hein KD, Mulliken JB, Kozakewich HPW, Upton J, Burrows PE. Venous malformations of skeletal muscle. Plast Reconstr Surg 2002; 110: 1625-1635.

https://doi.org/10.1097/00006534-200212000-00001 DOI: https://doi.org/10.1097/00006534-200212000-00001

Ros de San Pedro J, Cuartero Pérez B, Ferri Ñíguez B, Villanueva San Vicente V. Arteriovenous malformations of the temporalis muscle: a comprehensive review. Oper Neurosurg 2018; 14: 325-340.

https://doi.org/10.1093/ons/opx149 DOI: https://doi.org/10.1093/ons/opx149

Choi JH, Ro JY. The 2020 WHO classification of tumors of soft tissue: selected changes and new entities. Adv Anat Pathol 2021; 28: 44-58.

https://doi.org/10.1097/PAP.0000000000000284 DOI: https://doi.org/10.1097/PAP.0000000000000284

Hoeft S, Luettges J, Werner JA. Infiltrating angiolipoma of the M. temporalis. Auris Nasus Larynx 2000; 27: 265-269.

https://doi.org/10.1016/S0385-8146(99)00075-9 DOI: https://doi.org/10.1016/S0385-8146(99)00075-9

Kurek KC, Howard E, Tennant LB, Upton J, Alomari AI, Burrows PE, et al. PTEN hamartoma of soft tissue: a distinctive lesion in PTEN syndromes Am J Surg Pathol 2012; 36: 671-687.

https://doi.org/10.1097/PAS.0b013e31824dd86c DOI: https://doi.org/10.1097/PAS.0b013e31824dd86c

Stein-Wexler R. Pediatric soft tissue sarcomas. Semin Ultrasound CT MR 2011; 32: 470-488.

https://doi.org/10.1053/j.sult.2011.03.006 DOI: https://doi.org/10.1053/j.sult.2011.03.006

Wassef M, Blei F, Adams D, Alomari A, Baselga E, Berenstein A, et al. Vascular anomalies classification: recommendations from the International Society for the Study of Vascular Anomalies. Pediatrics 2015; 136: e203-204.

https://doi.org/10.1542/peds.2014-3673 DOI: https://doi.org/10.1542/peds.2014-3673

Couto JA, Huang AY, Konczyk DJ, Goss JA, Fishman SJ, Mulliken JB, et al. Somatic MAP2K1 mutations are associated with extracranial arteriovenous malformation. Am J Hum Genet 2017; 100: 546-554.

https://doi.org/10.1016/j.ajhg.2017.01.018 DOI: https://doi.org/10.1016/j.ajhg.2017.01.018

Al-Olabi L, Polubothu S, Dowsett K, Andrews KA, Stadnik P, Joseph AP, et al. Mosaic RAS/MAPK variants cause sporadic vascular malformations which respond to targeted therapy. J Clin Invest 2018; 128: 1496-1508.

https://doi.org/10.1172/JCI98589 DOI: https://doi.org/10.1172/JCI98589

Goss JA, Konczyk DJ, Smits PJ, Kozakewich HPW, Alomari AI, Al-Ibraheemi A, et al. Intramuscular fast-flow vascular anomaly contains somatic MAP2K1 and KRAS mutations. Angiogenesis 2019; 22: 547-552.

https://doi.org/10.1007/s10456-019-09678-w DOI: https://doi.org/10.1007/s10456-019-09678-w

Chen H, Xu B, Wang G, Guo Y, Hou K, Yu J, et al. Posterior occipital intramuscular hemangioma mimicking arteriovenous malformation: Case report. Medicine (Baltimore) 2019; 98: e14678.

https://doi.org/10.1097/MD.0000000000014678 DOI: https://doi.org/10.1097/MD.0000000000014678

Russo D, Fraitag S, Bruneau B, Stock N, Aillet S, Dupuy A, et al. Non-congenital dorsal tumefaction with rapid growth in a young child identified as an intramuscular hemangioma. JAAD Case Rep 2020; 6: 616-618.

https://doi.org/10.1016/j.jdcr.2020.04.039 DOI: https://doi.org/10.1016/j.jdcr.2020.04.039

Lipede C, Nikkhah D, Ashton R, Murphy G, Barnacle AM, Patel PA, et al. Management of Fibro-adipose Vascular Anomalies (FAVA) in paediatric practice. JPRAS Open 2021; 29: 71-81.

https://doi.org/10.1016/j.jpra.2021.05.002 DOI: https://doi.org/10.1016/j.jpra.2021.05.002

Dompmartin A, Acher A, Thibon P, Tourbach S, Hermans C, Deneys V, et al. Association of localized intravascular coagulopathy with venous malformations. Arch Dermatol 2008; 144: 873-877.

https://doi.org/10.1001/archderm.144.7.873 DOI: https://doi.org/10.1001/archderm.144.7.873

Colletti G, Biglioli F, Poli T, Dessy M, Cucurullo M, Petrillo M, et al. Vascular malformations of the orbit (lymphatic, venous, arteriovenous): diagnosis, management and results. J Craniomaxillofac Surg 2019; 47: 726-740.

https://doi.org/10.1016/j.jcms.2018.09.009 DOI: https://doi.org/10.1016/j.jcms.2018.09.009

Maruani A, Tavernier E, Boccara O, Mazereeuw-Hautier J, Leducq S, Bessis D, et al. Sirolimus (rapamycin) for slow-flow malformations in children: The observational-phase randomized clinical PERFORMUS trial. JAMA Dermatol 2021; 157: 1289-1298.

https://doi.org/10.1001/jamadermatol.2021.3459 DOI: https://doi.org/10.1001/jamadermatol.2021.3459

Chen RJ, Vrazas JI, Penington AJ. Surgical management of intramuscular venous malformations. J Pediatr Orthop 2021; 41: e67-e73.

https://doi.org/10.1097/BPO.0000000000001667 DOI: https://doi.org/10.1097/BPO.0000000000001667

Rabe E, Pannier F. Sclerotherapy in venous malformation. Phlebology 2013; 28: 188-191.

https://doi.org/10.1177/0268355513477282 DOI: https://doi.org/10.1177/0268355513477282

Yonehara Y, Nakatsuka T, Ichioka I, Takato T, Matsumoto S, Yamada A. Intramuscular haemangioma of the anterior chest wall. Br J Plast Surg 2000; 53: 257-259.

https://doi.org/10.1054/bjps.1999.3275 DOI: https://doi.org/10.1054/bjps.1999.3275

Lescura CM, de Andrade BAB, Bezerra KT, Agostini M, Ankha MVA, de Castro F, et al. Oral intramuscular hemangioma: report of three cases. J Cutan Pathol 2019; 46: 603-608.

https://doi.org/10.1111/cup.13482 DOI: https://doi.org/10.1111/cup.13482

Lyness RW, Williams R. Intramuscular haemangioma arising in the lateral rectus extraocular muscle: a case report and review of the published work. Orbit 1986; 5: 159-167.

https://doi.org/10.3109/01676838609036039 DOI: https://doi.org/10.3109/01676838609036039

Liu AS, Mulliken JB, Zurakowski D, Fishman SJ, Greene AK. Extracranial arteriovenous malformations: natural progression and recurrence after treatment Plast Reconstr Surg 2010; 125: 1185-1194.

https://doi.org/10.1097/PRS.0b013e3181d18070 DOI: https://doi.org/10.1097/PRS.0b013e3181d18070

Nicholson CL, Flanagan S, Murati M, Boull C, McGough E, Ameduri R, et al. Successful management of an arteriovenous malformation with trametinib in a patient with capillary-malformation arteriovenous malformation syndrome and cardiac compromise. Pediatr Dermatol 2022; 39: 316-319.

https://doi.org/10.1111/pde.14912 DOI: https://doi.org/10.1111/pde.14912

Additional Files

Published

2023-03-20

How to Cite

Orly, J., Bisdorff, A., Joly, A. ., Edee, A.-E. ., Tavernier, E., Herbreteau, D., … Maruani, A. (2023). Characteristics, Natural Course and Treatment of Intramuscular Capillary-type Haemangioma: A Systematic Literature Review. Acta Dermato-Venereologica, 103, adv00893. https://doi.org/10.2340/actadv.v103.4432

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