Venous malformations of skeletal muscle

Plastic and Reconstructive Surgery

Volumn 110, Issue 7, 2002, Pages 1625-1635

  Hein, Katherine D ^a   Mulliken, John B ^a   Kozakewich, Harry P W ^a   Upton, Joseph ^a   Burrows, Patricia E ^a  

^a BOSTON CHILDREN S HOSPITAL   (United States)

Author keywords

[No Author keywords available]

Indexed keywords

ACETYLSALICYLIC ACID;

ADOLESCENT; ANGIOGRAPHY; ARTICLE; CHILD; COMPRESSION THERAPY; COMPUTER ASSISTED TOMOGRAPHY; CONGENITAL BLOOD VESSEL MALFORMATION; CONSERVATIVE TREATMENT; DIAGNOSTIC IMAGING; ECHOGRAPHY; EXCISION; FEMALE; HISTOPATHOLOGY; HUMAN; HUMAN TISSUE; MAJOR CLINICAL STUDY; MALE; NUCLEAR MAGNETIC RESONANCE IMAGING; PRIORITY JOURNAL; SCLEROTHERAPY; SKELETAL MUSCLE; SYMPTOMATOLOGY; VEIN MALFORMATION; X RAY;

EID: 0036902251     PISSN: 00321052     EISSN: None     Source Type: Journal    
DOI: 10.1097/00006534-200212000-00001     Document Type: Article

References (43)

1. Mulliken, J. B., and Glowacki, J. Hemangiomas and vascular malformations in infants and children: A classification based on endothelial characteristics. Plast. Reconstr. Surg. 69: 412, 1982.
2. Mulliken, J. B., and Young, A. E. Vascular Birthmarks: Hemangiomas and Malformations. Philadelphia: Saunders, 1988.
3. Vikkula, M., Boon, L. M., Mulliken, J. B., et al. Molecular basis of vascular anomalies. Trends Cardiovasc. Med. 8: 281, 1998.
4. Enjolras, O., and Mulliken, J. B. Vascular tumors and vascular malformations: New issues. Adv. Dermatol. 13: 375, 1998.
5. Enjolras, O., Wassef, M., Mazoyer, E., et al. Infants with Kasabach-Merritt syndrome do not have "true" hemangiomas. J. Pediatr. 130: 631, 1997.
6. Sarkar, M., Mulliken, J. B., Kozakewich, H. P. W., Robertson, R. L., and Burrows, P. E. Thrombocytopenic coagulopathy (Kasabach-Merritt phenomenon) is associated with kaposiform hemangioendothelioma and not with common infantile hemangioma. Plast. Reconstr. Surg. 100: 1377, 1997.
7. Resnick, S. D., Lacey, S., and Jones, G. Hemorrhagic complications in a rapidly growing congenital hemangiopericytoma. Pediatr. Dermatol. 10: 267, 1993.
8. Allen, P. W., and Enzinger, F. M. Hemangioma of skeletal muscle: An analysis of 89 cases. Cancer 29: 8, 1972.
9. Calonje, E., and Flectcher, C. D. M. Tumors of blood vessels and lymphatics. In C. D. M. Fletcher (Ed.), Diagnostic Histopathology of Tumors, 2nd Ed. New York: Churchill Livingstone, 2000. Pp. 59-60.
10. Kempson, R. L., Fletcher, C. D. M., Owens, H. L., et al. Atlas of Tumor Pathology (Third Series Fascicle 30). Washington, D.C.: Armed Forces Institute of Pathology, 2001. Pp. 325-358.
11. Mulliken, J. B. Cutaneous vascular anomalies. Semin. Vasc. Surg. 6: 204, 1993.
12. Rosai, J. (Ed.). Ackerman's Surgical Pathology, 8th Ed. St. Louis: Mosby-Year Book, 1996. P. 182.
13. Rigamonti, D., Hadley, M. N., Drayer, B. P., et al. Cerebral cavernous malformations: Incidence and familial occurrence. N. Engl. J. Med. 319: 343, 1988.
14. Stueber, K., and Hafiz, M. A. Hemangioma of the masseter muscle: A case report and review of the literature. Ann. Plast. Surg. 16: 257, 1986.
15. Yuh, W. T. C., Kathol, M. H., Sein, M. A., Ehara, S., and Chiu, L. Hemangiomas of skeletal muscle: MR findings in five patients. A.J.R. Am. J. Roentgenol. 149: 765, 1987.
16. Joehl, R.J., Miller, S. H., Davis, T. S., and Graham, W. P., III. Hemangioma of the temporalis muscle: A case report and review of the literature. Ann. Plast. Surg. 3: 273, 1979.
17. Welsh, D., and Hengerer, A. S. The diagnosis and treatment of intramuscular hemangiomas of the masseter muscle. Am. J. Otolaryngol. 1: 186, 1980.
18. Jenner, G., Soderlund, V., Bauer, H. F. C., and Brosijo, O. MR imaging of skeletal muscle hemangiomas: A report of 16 cases. Acta Radiol. 37: 140, 1996.
19. Harar, R. P. S., Kalan, A., Brown, C. L., and Kenyon, G. S. A unique tumour of the geniohyoid muscle: An intramuscular haemangioma. J. Laryngol. Otol. 111: 769, 1997.
20. Sharma, B. S., Chari, P. S., Joshi, K., and Rajvanshi, A. Hemangioma of the temporalis muscle. Ann. Otol. Rhinol. Laryngol. 100: 76, 1991.
21. Weiss, S. W., and Goldblum, J. R. Benign tumors and tumor-like lesions of blood vesels. In S. W. Weiss and J. F. Goldblum (Eds.), Enzinger and Weiss's Soft Tissue Tumors, 4th Ed. St. Louis: Mosby-Year Book, 1995. Pp. 869-872.
22. Weiss, S. W., and Enzinger F. M. Spindle cell hemangioendothelioma: A low-grade angiosarcoma resembling cavernous hemangioma and Kaposi's sarcoma. Am. J. Surg. Pathol. 10: 521, 1986.
23. Fletcher, C. D. M., Beham, A., and Schmid, C. Spindle cell haemangioendothelioma: A clinicopathological and immunohistochemical study indicative of a nonneoplastic lesion. Histopathology 18: 291, 1991.
24. Imayama, S., Murakamai, Y., Hashimoto, H., and Hori,Y. Spindle cell hemangioendothelioma exhibits the ultrastructural features of reactive vascular proliferation rather than of angiosarcoma. Am. J. Clin. Pathol. 97: 279, 1992.
25. Eltorky, M., McChesney, T., Sebes, J., and Hall, J. C. Spindle cell hemangioendothelioma: Report of three cases and review of the literature. J. Dermatol. Surg. Oncol. 20: 196, 1994.
26. Perkins, P., and Weiss, S. W. Spindle cell hemangioendothelioma: An analysis of 78 cases with reassessment of its pathogenesis and biologic behavior. Am. J. Surg. Pathol. 20: 1196, 1996.
27. Takahashi, K., Mulliken, J. B., Kozakewich, H. P. W., Rogers, R. A., Folkman, J., and Ezekowitz, R. A. B. Cellular markers that distinguish the phases of hemangioma during infancy and childhood. J. Clin. Invest. 93: 2357, 1994.
28. North, P. E., Waner, M., Mizeracki, A., and Mihm, M. C., Jr. GLUT1: A newly discovered immunohistochemical marker for juvenile hemangiomas. Hum. Pathol. 31: 11, 2000.
29. Vikkula, M., Boon, L. M., Carraway, K. L., III, et al. Vascular dysmorphogenesis caused by activating mutation in the receptor tyrosine kinase TIE2. Cell 87: 1181, 1996.
30. Boon, L. M., Mulliken, J. B., Vikkula, M., et al. Assignment of a locus for dominantly inherited venous malformations to chromosome 9p. Hum. Mol. Genet. 3: 1583, 1994.
31. Boon, L. M., Brouillard, P., Irrthum, A., et al. A gene for inherited cutaneous venous anomalies ("glomangiomas") localizes to chromosome 1p21-22. Am. J. Hum. Genet. 65: 125, 1999.
32. Brouillard, P., Boon, L. M., Mulliken, J. B., et al. Mutations in a novel factor, glomulin, are responsible for glomuvenous malformations ("glomangiomas"). Am. J. Hum. Genet. 70: 866, 2002.
33. Dubovsky, J., Zabramski, J. M., Kurth, J., et al. A gene responsible for cavernous malformations of the brain maps to chromosome 7q. Hum. Mol. Genet. 4: 453, 1995.
34. Laberge-le Couteulx, S., Jung, H. H., Labauge, P., et al. Truncation mutations in CCM1, encoding KRIT1, cause hereditary cavernous angiomas. Nat. Genet. 23: 189, 1999.
35. Rak, K. M., Yakes, W. F., Ray, R. L., et al. MR imaging of symptomatic peripheral vascular malformations. A.J.R. Am. J. Roentgenol. 159: 107, 1992.
36. Burrows, P. E., Mulliken, J. B., Fellows, K. E., and Strand, R. D. Childhood hemangiomas and vascular malformations: Angiographic differentiation. A.J.R. Am. J. Roentgenol. 141: 483, 1983.
37. Yakes, W. F., and Parker, S. H. Diagnosis and management of vascular anomalies. In W. R. Castaneda-Zuniga and S. M. Tadavarthy (Eds.), Interventional Radiology, 3rd Ed. Baltimore: Williams & Wilkins, 1997. Pp. 118-121.
38. Yakes, W.F. Diagnosis and management of venous malformations. In S. J. Savader and S. O. Trerotola (Eds.), Venous Interventional Radiology with Clinical Perspectives. New York: Thieme, 1996. Pp. 139-150.
39. Upton, J., Coombs, C. J., Mulliken, J. B., Burrows, P. E., and Pap, S. Vascular malformations of the upper limb: A review of 270 patients. J. Hand Surg. (Am.) 24: 1019, 1999.
40. Upton, J., Mulliken, J. B., and Murray, J. E. The classification and rationale for management of vascular anomalies of the upper extremity. J. Hand Surg. (Am.) 10: 970, 1985.
41. Upton, J. Vascular malformation of the upper limb. In J. B. Mulliken and A. E. Young (Eds.), Vascular Birthmarks: Hemangiomas and Malformations. Philadelphia: Saunders, 1988. Pp. 343-380.
42. Upton, J. The recognition and treatment of vascular tumors and malformations in children. In A. Gupta, S. P. J. Kay, and L. R. Scheker (Eds.), The Growing Hand: Diagnosis and Management of the Upper Extremity in Children. London: Mosby, 2000. Pp. 831-856.
43. Berenguer, B., Burrows, P. E., Zurakowski, D., and Mulliken, J. B. Sclerotherapy of craniofacial venous malformations: Complications and results. Plast. Reconstr. Surg. 104: 1, 1999.