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Erschienen in: Virchows Archiv 2/2009

01.02.2009 | Original Article

Vascular lesions of bone in children, adolescents, and young adults. A clinicopathologic reappraisal and application of the ISSVA classification

verfasst von: Elisabeth Bruder, Antonio R. Perez-Atayde, Gernot Jundt, Ahmad I. Alomari, Johannes Rischewski, Steven J. Fishman, John B. Mulliken, Harry P. W. Kozakewich

Erschienen in: Virchows Archiv | Ausgabe 2/2009

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Abstract

Vascular lesions of bone are rare and their terminology is not standardized. Herein, we report 77 patients with such lesions in order to characterize their morphologic spectrum and the applicability of the International Society for the Study of Vascular Anomalies (ISSVA) classification. In this system, malformations are structural anomalies distinguishable from tumors, which are proliferative. The radiologic images/reports and pathologic materials from all patients were reviewed. All lesions were either restricted to bone or had minimal contiguous soft tissue involvement with the exception of some multifocal lymphatic lesions that extensively affected soft tissue and/or viscera. We found that certain lesions of bone often regarded as tumors should be classified as malformations. Malformations (n = 46) were more common than tumors (n = 31); lymphatic and venous malformations were equally frequent. In the tumor category, hemangioendothelioma and epithelioid hemangioma were the most common. We also describe new vascular entities that arise in or involve bone. Utilizing the ISSVA approach, the diverse and often contradictory terminology of vascular lesions of bone can be largely eliminated. Standardized nomenclature is critical for scientific communication and patient management, and we hereby recommend the ISSVA classification be applied to vascular lesions of bone, just as for skin, soft tissue, and viscera.
Literatur
1.
Zurück zum Zitat Fechner RE, Mills SE (1993) Tumors of the bones and joints. Atlas of tumor pathology. Armed Forces Institute of Pathology Washington DC 1993 Fechner RE, Mills SE (1993) Tumors of the bones and joints. Atlas of tumor pathology. Armed Forces Institute of Pathology Washington DC 1993
2.
Zurück zum Zitat Dorfman HD, Czerniac B (1998) Bone tumors. Mosby, St. Louis 1998 Dorfman HD, Czerniac B (1998) Bone tumors. Mosby, St. Louis 1998
3.
Zurück zum Zitat Unni KK (1996) Dahlin’s bone tumors. General aspects and data on 11,087 cases. Lippincott Raven, Philadelphia 1996 Unni KK (1996) Dahlin’s bone tumors. General aspects and data on 11,087 cases. Lippincott Raven, Philadelphia 1996
4.
Zurück zum Zitat Schmorl G, Junghanns H (1959) The human spine in health and disease. Grune & Stratton, New York 1959 Schmorl G, Junghanns H (1959) The human spine in health and disease. Grune & Stratton, New York 1959
5.
Zurück zum Zitat Enjolras O, Mulliken JB (1997) Vascular tumors and vascular malformations (new issues). Adv Dermatol 13:375–423PubMed Enjolras O, Mulliken JB (1997) Vascular tumors and vascular malformations (new issues). Adv Dermatol 13:375–423PubMed
6.
Zurück zum Zitat Bruder E, Kozakewich H (2004) Skeletal vascular lesions in childhood and adolescence. Pathologe 25:311–316PubMed Bruder E, Kozakewich H (2004) Skeletal vascular lesions in childhood and adolescence. Pathologe 25:311–316PubMed
7.
Zurück zum Zitat Frick H, Leonhardt H, Starck D (1992) Allgemeine anatomie, spezielle anatomy I. Extremitaeten-Rumpfwand. Thieme, Stuttgart 1992 Frick H, Leonhardt H, Starck D (1992) Allgemeine anatomie, spezielle anatomy I. Extremitaeten-Rumpfwand. Thieme, Stuttgart 1992
8.
Zurück zum Zitat Standring S, Ellis H, Healey JC et al (2005) Gray’s anatomy. Elsevier Churchill Livingstone, Edinburgh Standring S, Ellis H, Healey JC et al (2005) Gray’s anatomy. Elsevier Churchill Livingstone, Edinburgh
9.
Zurück zum Zitat Lawley LP, Cerimele F, Weiss SW et al (2005) Expression of Wilms tumor 1 gene distinguishes vascular malformations from proliferative endothelial lesions. Arch Dermatol 141:1297–1300PubMedCrossRef Lawley LP, Cerimele F, Weiss SW et al (2005) Expression of Wilms tumor 1 gene distinguishes vascular malformations from proliferative endothelial lesions. Arch Dermatol 141:1297–1300PubMedCrossRef
10.
Zurück zum Zitat Nascimento AG, Keeney GL, Sciot R et al (1997) Polymorphous hemangioendothelioma: a report of two cases, one affecting extranodal soft tissues, and review of the literature. Am J Surg Pathol 21:1083–1089PubMedCrossRef Nascimento AG, Keeney GL, Sciot R et al (1997) Polymorphous hemangioendothelioma: a report of two cases, one affecting extranodal soft tissues, and review of the literature. Am J Surg Pathol 21:1083–1089PubMedCrossRef
11.
Zurück zum Zitat Enjolras O, Mulliken JB, Boon LM et al (2001) Noninvoluting congenital hemangioma: a rare cutaneous vascular anomaly. Plast Reconstr Surg 107:1647–1654PubMedCrossRef Enjolras O, Mulliken JB, Boon LM et al (2001) Noninvoluting congenital hemangioma: a rare cutaneous vascular anomaly. Plast Reconstr Surg 107:1647–1654PubMedCrossRef
12.
Zurück zum Zitat Fletcher CD, Unni KK, Mertens F (2002) World Health Organization classification of tumours. Pathology and genetics of tumours of soft tissue and bone. IARC Press, Lyon 2002 Fletcher CD, Unni KK, Mertens F (2002) World Health Organization classification of tumours. Pathology and genetics of tumours of soft tissue and bone. IARC Press, Lyon 2002
13.
Zurück zum Zitat Mirra JM, Picci B, Gold RH (1989) Bone tumors. Clinical, radiologic and pathologic correlations. Lea & Febiger, Philadelphia 1989 Mirra JM, Picci B, Gold RH (1989) Bone tumors. Clinical, radiologic and pathologic correlations. Lea & Febiger, Philadelphia 1989
14.
15.
Zurück zum Zitat Meijer-Jorna LB, van der Loos CM, de Boer OJ et al (2007) Microvascular proliferation in congenital vascular malformations of skin and soft tissue. J Clin Pathol 60:798–803PubMedCrossRef Meijer-Jorna LB, van der Loos CM, de Boer OJ et al (2007) Microvascular proliferation in congenital vascular malformations of skin and soft tissue. J Clin Pathol 60:798–803PubMedCrossRef
16.
Zurück zum Zitat Sure U, Butz N, Schlegel J et al (2001) Endothelial proliferation, neoangiogenesis, and potential de novo generation of cerebrovascular malformations. J Neurosurg 94:972–977PubMed Sure U, Butz N, Schlegel J et al (2001) Endothelial proliferation, neoangiogenesis, and potential de novo generation of cerebrovascular malformations. J Neurosurg 94:972–977PubMed
17.
Zurück zum Zitat Sure U, Freman S, Bozinov O et al (2005) Biological activity of adult cavernous malformations: a study of 56 patients. J Neurosurg 102:342–347PubMedCrossRef Sure U, Freman S, Bozinov O et al (2005) Biological activity of adult cavernous malformations: a study of 56 patients. J Neurosurg 102:342–347PubMedCrossRef
18.
Zurück zum Zitat Jaffe HL (1958) Tumors and tumorous conditions of bones and joints. Lea & Febiger, Philadelphia 1958 Jaffe HL (1958) Tumors and tumorous conditions of bones and joints. Lea & Febiger, Philadelphia 1958
19.
Zurück zum Zitat Huvos AG (1991) Bone tumors: diagnosis, treatment and prognosis. Saunders, Philadelphia 1991 Huvos AG (1991) Bone tumors: diagnosis, treatment and prognosis. Saunders, Philadelphia 1991
20.
Zurück zum Zitat Greene AK, Rogers GF, Mulliken JB (2007) Intraosseous “hemangiomas” are malformations and not tumors. Plast Reconstr Surg 119:1949–1950PubMedCrossRef Greene AK, Rogers GF, Mulliken JB (2007) Intraosseous “hemangiomas” are malformations and not tumors. Plast Reconstr Surg 119:1949–1950PubMedCrossRef
21.
Zurück zum Zitat Chen L, Zhang CL, Tang TS (2007) Cement vertebroplasty combined with ethanol injection in the treatment of vertebral hemangioma. Chin Med J (Engl) 120:1136–1139 Chen L, Zhang CL, Tang TS (2007) Cement vertebroplasty combined with ethanol injection in the treatment of vertebral hemangioma. Chin Med J (Engl) 120:1136–1139
22.
Zurück zum Zitat Doppman JL, Oldfield EH, Heiss JD (2000) Symptomatic vertebral hemangiomas: treatment by means of direct intralesional injection of ethanol. Radiology 214:341–348PubMed Doppman JL, Oldfield EH, Heiss JD (2000) Symptomatic vertebral hemangiomas: treatment by means of direct intralesional injection of ethanol. Radiology 214:341–348PubMed
23.
Zurück zum Zitat Giaoui L, Princ G, Chiras J et al (2003) Treatment of vascular malformations of the mandible: a description of 12 cases. Int J Oral Maxillofac Surg 32:132–136PubMedCrossRef Giaoui L, Princ G, Chiras J et al (2003) Treatment of vascular malformations of the mandible: a description of 12 cases. Int J Oral Maxillofac Surg 32:132–136PubMedCrossRef
24.
Zurück zum Zitat Goyal M, Mishra NK, Sharma A et al (1999) Alcohol ablation of symptomatic vertebral hemangiomas. AJNR Am J Neuroradiol 20:1091–1096PubMed Goyal M, Mishra NK, Sharma A et al (1999) Alcohol ablation of symptomatic vertebral hemangiomas. AJNR Am J Neuroradiol 20:1091–1096PubMed
25.
Zurück zum Zitat Persky MS, Yoo HJ, Berenstein A (2003) Management of vascular malformations of the mandible and maxilla. Laryngoscope 113:1885–1892PubMedCrossRef Persky MS, Yoo HJ, Berenstein A (2003) Management of vascular malformations of the mandible and maxilla. Laryngoscope 113:1885–1892PubMedCrossRef
26.
Zurück zum Zitat Casanova D, Boon LM, Vikkula M (2006) Venous malformations: clinical characteristics and differential diagnosis. Ann Chir Plast Esthet 51:373–387PubMedCrossRef Casanova D, Boon LM, Vikkula M (2006) Venous malformations: clinical characteristics and differential diagnosis. Ann Chir Plast Esthet 51:373–387PubMedCrossRef
27.
Zurück zum Zitat Maffucci AM (1881) Di un caso di encondroma ed angioma multiplo. Contribuzione alla genesi embrionale dei tumori. Mov Med Chir Napoli 13:399–412 Maffucci AM (1881) Di un caso di encondroma ed angioma multiplo. Contribuzione alla genesi embrionale dei tumori. Mov Med Chir Napoli 13:399–412
28.
Zurück zum Zitat North PE, Waner M, Mizeracki A et al (2000) GLUT1: a newly discovered immunohistochemical marker for juvenile hemangiomas. Hum Pathol 31:11–22PubMedCrossRef North PE, Waner M, Mizeracki A et al (2000) GLUT1: a newly discovered immunohistochemical marker for juvenile hemangiomas. Hum Pathol 31:11–22PubMedCrossRef
29.
Zurück zum Zitat Koulouris G, Rao P (2005) Multiple congenital cranial hemangiomas. Skeletal Radiol 34:485–489PubMedCrossRef Koulouris G, Rao P (2005) Multiple congenital cranial hemangiomas. Skeletal Radiol 34:485–489PubMedCrossRef
30.
Zurück zum Zitat Vikkula M, Boon LM, Mulliken JB (2001) Molecular genetics of vascular malformations. Matrix Biol 20:327–335PubMedCrossRef Vikkula M, Boon LM, Mulliken JB (2001) Molecular genetics of vascular malformations. Matrix Biol 20:327–335PubMedCrossRef
31.
Zurück zum Zitat Flores-Vargas A, Vargas SO, Debelenko LV et al (2008) Comparative analysis of D2-40 and LYVE-1 immunostaining in lymphatic malformations. Lymphology 41:103–110 Flores-Vargas A, Vargas SO, Debelenko LV et al (2008) Comparative analysis of D2-40 and LYVE-1 immunostaining in lymphatic malformations. Lymphology 41:103–110
32.
Zurück zum Zitat Hirakawa S, Detmar M (2004) New insights into the biology and pathology of the cutaneous lymphatic system. J Dermatol Sci 35:1–8PubMedCrossRef Hirakawa S, Detmar M (2004) New insights into the biology and pathology of the cutaneous lymphatic system. J Dermatol Sci 35:1–8PubMedCrossRef
33.
Zurück zum Zitat Coley BL (1949) Neoplasms of bone and related conditions. Their etiology, pathogenesis, diagnosis and treatment. Paul B. Hoeber, New York 1949 Coley BL (1949) Neoplasms of bone and related conditions. Their etiology, pathogenesis, diagnosis and treatment. Paul B. Hoeber, New York 1949
34.
Zurück zum Zitat Gorham LW, Stout AP (1955) Massive osteolysis (acute spontaneous absorption of bone, phantom bone, disappearing bone); its relation to hemangiomatosis. J Bone Joint Surg Am 37-A:985–1004PubMed Gorham LW, Stout AP (1955) Massive osteolysis (acute spontaneous absorption of bone, phantom bone, disappearing bone); its relation to hemangiomatosis. J Bone Joint Surg Am 37-A:985–1004PubMed
35.
Zurück zum Zitat Gorham LW, Wright AW, Shultz HH et al (1954) Disappearing bones: a rare form of massive osteolysis; report of two cases, one with autopsy findings. Am J Med 17:674–682PubMedCrossRef Gorham LW, Wright AW, Shultz HH et al (1954) Disappearing bones: a rare form of massive osteolysis; report of two cases, one with autopsy findings. Am J Med 17:674–682PubMedCrossRef
36.
Zurück zum Zitat Colucci S, Taraboletti G, Primo L et al (2006) Gorham-Stout syndrome: a monocyte-mediated cytokine propelled disease. J Bone Miner Res 21:207–218PubMedCrossRef Colucci S, Taraboletti G, Primo L et al (2006) Gorham-Stout syndrome: a monocyte-mediated cytokine propelled disease. J Bone Miner Res 21:207–218PubMedCrossRef
37.
Zurück zum Zitat Hirayama T, Sabokbar A, Itonaga I et al (2001) Cellular and humoral mechanisms of osteoclast formation and bone resorption in Gorham-Stout disease. J Pathol 195:624–630PubMedCrossRef Hirayama T, Sabokbar A, Itonaga I et al (2001) Cellular and humoral mechanisms of osteoclast formation and bone resorption in Gorham-Stout disease. J Pathol 195:624–630PubMedCrossRef
38.
Zurück zum Zitat O’Connell JX, Kattapuram SV, Mankin HJ et al (1993) Epithelioid hemangioma of bone. A tumor often mistaken for low-grade angiosarcoma or malignant hemangioendothelioma. Am J Surg Pathol 17:610–617PubMedCrossRef O’Connell JX, Kattapuram SV, Mankin HJ et al (1993) Epithelioid hemangioma of bone. A tumor often mistaken for low-grade angiosarcoma or malignant hemangioendothelioma. Am J Surg Pathol 17:610–617PubMedCrossRef
39.
Zurück zum Zitat Evans HL, Raymond AK, Ayala AG (2003) Vascular tumors of bone: a study of 17 cases other than ordinary hemangioma, with an evaluation of the relationship of hemangioendothelioma of bone to epithelioid hemangioma, epithelioid hemangioendothelioma, and high-grade angiosarcoma. Hum Pathol 34:680–689PubMedCrossRef Evans HL, Raymond AK, Ayala AG (2003) Vascular tumors of bone: a study of 17 cases other than ordinary hemangioma, with an evaluation of the relationship of hemangioendothelioma of bone to epithelioid hemangioma, epithelioid hemangioendothelioma, and high-grade angiosarcoma. Hum Pathol 34:680–689PubMedCrossRef
40.
Zurück zum Zitat O’Connell JX, Nielsen GP, Rosenberg AE (2001) Epithelioid vascular tumors of bone: a review and proposal of a classification scheme. Adv Anat Pathol 8:74–82PubMedCrossRef O’Connell JX, Nielsen GP, Rosenberg AE (2001) Epithelioid vascular tumors of bone: a review and proposal of a classification scheme. Adv Anat Pathol 8:74–82PubMedCrossRef
41.
Zurück zum Zitat Keel SB, Rosenberg AE (1999) Hemorrhagic epithelioid and spindle cell hemangioma: a newly recognized, unique vascular tumor of bone. Cancer 85:1966–1972PubMed Keel SB, Rosenberg AE (1999) Hemorrhagic epithelioid and spindle cell hemangioma: a newly recognized, unique vascular tumor of bone. Cancer 85:1966–1972PubMed
42.
Zurück zum Zitat Mendlick MR, Nelson M, Pickering D et al (2001) Translocation t(1;3)(p36.3;q25) is a nonrandom aberration in epithelioid hemangioendothelioma. Am J Surg Pathol 25:684–687PubMedCrossRef Mendlick MR, Nelson M, Pickering D et al (2001) Translocation t(1;3)(p36.3;q25) is a nonrandom aberration in epithelioid hemangioendothelioma. Am J Surg Pathol 25:684–687PubMedCrossRef
43.
Zurück zum Zitat Theurillat JP, Vavricka SR, Went P et al (2003) Morphologic changes and altered gene expression in an epithelioid hemangioendothelioma during a ten-year course of disease. Pathol Res Pract 199:165–170PubMedCrossRef Theurillat JP, Vavricka SR, Went P et al (2003) Morphologic changes and altered gene expression in an epithelioid hemangioendothelioma during a ten-year course of disease. Pathol Res Pract 199:165–170PubMedCrossRef
44.
Zurück zum Zitat Lezama-del Valle P, Gerald WL, Tsai J et al (1998) Malignant vascular tumors in young patients. Cancer 83:1634–1639PubMedCrossRef Lezama-del Valle P, Gerald WL, Tsai J et al (1998) Malignant vascular tumors in young patients. Cancer 83:1634–1639PubMedCrossRef
45.
Zurück zum Zitat Folpe AL, Veikkola T, Valtola R et al (2000) Vascular endothelial growth factor receptor-3 (VEGFR-3): a marker of vascular tumors with presumed lymphatic differentiation, including Kaposi’s sarcoma, kaposiform and Dabska-type hemangioendotheliomas, and a subset of angiosarcomas. Mod Pathol 13:180–185PubMedCrossRef Folpe AL, Veikkola T, Valtola R et al (2000) Vascular endothelial growth factor receptor-3 (VEGFR-3): a marker of vascular tumors with presumed lymphatic differentiation, including Kaposi’s sarcoma, kaposiform and Dabska-type hemangioendotheliomas, and a subset of angiosarcomas. Mod Pathol 13:180–185PubMedCrossRef
46.
Zurück zum Zitat Debelenko LV, Marler JJ, Perez-Atayde AR et al (Abstract) (2004) Kaposiform lymphangiomatosis: an aggressive variant of lymphangiomatosis. Mod Pathol 17:267 Debelenko LV, Marler JJ, Perez-Atayde AR et al (Abstract) (2004) Kaposiform lymphangiomatosis: an aggressive variant of lymphangiomatosis. Mod Pathol 17:267
47.
Zurück zum Zitat Zukerberg LR, Nickoloff BJ, Weiss SW (1993) Kaposiform hemangioendothelioma of infancy and childhood. An aggressive neoplasm associated with Kasabach-Merritt syndrome and lymphangiomatosis. Am J Surg Pathol 17:321–328PubMedCrossRef Zukerberg LR, Nickoloff BJ, Weiss SW (1993) Kaposiform hemangioendothelioma of infancy and childhood. An aggressive neoplasm associated with Kasabach-Merritt syndrome and lymphangiomatosis. Am J Surg Pathol 17:321–328PubMedCrossRef
48.
Zurück zum Zitat Mac-Moune Lai F, To KF, Choi PC et al (2001) Kaposiform hemangioendothelioma: five patients with cutaneous lesion and long follow-up. Mod Pathol 14:1087–1092PubMedCrossRef Mac-Moune Lai F, To KF, Choi PC et al (2001) Kaposiform hemangioendothelioma: five patients with cutaneous lesion and long follow-up. Mod Pathol 14:1087–1092PubMedCrossRef
Metadaten
Titel
Vascular lesions of bone in children, adolescents, and young adults. A clinicopathologic reappraisal and application of the ISSVA classification
verfasst von
Elisabeth Bruder
Antonio R. Perez-Atayde
Gernot Jundt
Ahmad I. Alomari
Johannes Rischewski
Steven J. Fishman
John B. Mulliken
Harry P. W. Kozakewich
Publikationsdatum
01.02.2009
Verlag
Springer-Verlag
Erschienen in
Virchows Archiv / Ausgabe 2/2009
Print ISSN: 0945-6317
Elektronische ISSN: 1432-2307
DOI
https://doi.org/10.1007/s00428-008-0709-3

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