Complex combined vascular malformations and vascular malformation syndromes affecting the extremities in children

Seminars in Musculoskeletal Radiology

Volumn 13, Issue 3, 2009, Pages 255-276

  Lobo Mueller, Edrise ^a,b   Amaral, Joao G ^a  

^a HOSPITAL FOR SICK CHILDREN   (Canada)

^b UNIVERSITY OF TORONTO   (Canada)

Author keywords

Complex vascular anomalies; Gorham Stout disease; Klippel Tr naunay syndrome; Maffucci's syndrome; Magnetic resonance imaging; Parkes Weber syndrome; Proteus syndrome; Vascular malformations

Indexed keywords

ALKALINE PHOSPHATASE; ALPHA2B INTERFERON; ANTIBIOTIC AGENT; BISPHOSPHONIC ACID DERIVATIVE; D DIMER; LOW MOLECULAR WEIGHT HEPARIN; MEDRONATE TECHNETIUM TC 99M;

ALKALINE PHOSPHATASE BLOOD LEVEL; ANGIOOSTEOHYPERTROPHY SYNDROME; BANNAYAN RILEY RUVALCABA SYNDROME; BLEEDING; BLOOD CLOTTING DISORDER; BONE SCINTISCANNING; CHRONIC VEIN INSUFFICIENCY; CLINICAL FEATURE; COMPRESSION GARMENT; COMPRESSION THERAPY; CONGENITAL BLOOD VESSEL MALFORMATION; CONVENTIONAL ANGIOGRAPHY; CUTIS MARMORATA TELANGIECTATICA CONGENITA; DEEP VEIN THROMBOSIS; DIAGNOSTIC IMAGING; DIAGNOSTIC PROCEDURE; DIFFUSE EXTENSIVE VENOUS MALFORMATION; DISEASE COURSE; DISSEMINATED INTRAVASCULAR CLOTTING; EPIPHYSIODESIS; EXCISION; FETUS ECHOGRAPHY; GENE MUTATION; GORHAM STOUT DISEASE; GRAM NEGATIVE SEPSIS; HISTOPATHOLOGY; HUMAN; INFECTION; LIMB MALFORMATION; LUNG EMBOLISM; LYMPHATIC DRAINAGE; LYMPHEDEMA; MULTIPLE CANCER; MUSCULOSKELETAL SYSTEM MALFORMATION; NUCLEAR MAGNETIC RESONANCE IMAGING; ORTHOPEDIC SHOE; ORTHOPEDIC SURGERY; OSSIFICATION; OSTEOCHONDROMA; OSTEOLYSIS; PATIENT CARE; PHLEBOGRAPHY; PHYSIOTHERAPY; PROGNOSIS; PULSED DYE LASER; RADIATION DOSE; RADIOGRAPHY; REVIEW; SCLEROTHERAPY; THROMBOPHLEBITIS; THROMBUS; TISSUE SPECIFICITY; ULTRASOUND; VARICOSIS; VASCULAR CAPACITY; VEIN MALFORMATION;

BLOOD VESSELS; CHILD; ENCHONDROMATOSIS; EXTREMITIES; HUMANS; KLIPPEL-TRENAUNAY-WEBER SYNDROME; MAGNETIC RESONANCE IMAGING; PROTEUS SYNDROME;

EID: 70350448128     PISSN: 10897860     EISSN: 1098898X     Source Type: Journal    
DOI: 10.1055/s-0029-1237692     Document Type: Review

References (122)

1. Enjolras O, Wassef M, Chapot R. Introduction: ISSVA classification. In: Color Atlas of Vascular Tumors and Vascular Malformations. New York, NY Cambridge University Press 2007
2. Alomari A I. A truly unusual overgrowth syndrome: an alternative diagnosis to Klippel-Trénaunay-Weber syndrome. Intern Med 2009 48 (6) 493-494 author reply 495
3. Biesecker L G., Happle R, Mulliken J B. et al. Proteus syndrome: diagnostic criteria, differential diagnosis, and patient evaluation. Am J Med Genet 1999 84 (5) 389-395
4. Burrows P E., Mason K P. Percutaneous treatment of low flow vascular malformations. J Vasc Interv Radiol 2004 15 (5) 431-445
5. Enjolras O, Chapot R, Merland J J. Vascular anomalies and the growth of limbs: a review. J Pediatr Orthop B 2004 13 (6) 349-357
6. Mulliken J B., Young A E. Combined vascular anomalies. In: Vascular Birthmarks: Hemangiomas and Vascular Malformations. Philadelphia, PA WB Saunders 1988 246-274
7. Gloviczki P, Driscoll D J. Klippel-Trenaunay syndrome: current management. Phlebology 2007 22 (6) 291-298
8. Jacob A G., Driscoll D J., Shaughnessy W J., Stanson A W., Clay R P., Gloviczki P. Klippel-Trénaunay syndrome: spectrum and management. Mayo Clin Proc 1998 73 (1) 28-36
9. Garzon M C., Huang J T., Enjolras O, Frieden I J. Vascular malformations. Part II: associated syndromes. J Am Acad Dermatol 2007 56 (4) 541-564
10. Gloviczki P, Hollier L H., Telander R L., Kaufman B, Bianco A J., Stickler G B. Surgical implications of Klippel-Trenaunay syndrome. Ann Surg 1983 197 (3) 353-362
11. Berry S A., Peterson C, Mize W et al. Klippel-Trenaunay syndrome. Am J Med Genet 1998 79 (4) 319-326
12. McGrory B J., Amadio P C. Klippel-Trenaunay syndrome: orthopaedic considerations. Orthop Rev 1993 22 (1) 41-50
13. Noel A A., Gloviczki P, Cherry K J. Jr, Rooke T W., Stanson A W., Driscoll D J. Surgical treatment of venous malformations in Klippel- Trénaunay syndrome. J Vasc Surg 2000 32 (5) 840-847
14. Mattassi R, Vaghi M. Vascular bone syndromeangio-osteodystrophy: current concepts. Phlebology 2007 22 (6) 287-290
15. Delis K T., Gloviczki P, Wennberg P W., Rooke T W., Driscoll D J. Hemodynamic impairment, venous segmental disease, and clinical severity scoring in limbs with Klippel-Trenaunay syndrome. J Vasc Surg 2007 45 (3) 561-567
16. Samlaska C P., Gagliardi J A. Diffuse venous malformation with intraosseous involvement. Hawaii Med J 1994 53 (8) 218-221
17. Laor T, Burrows P E. Congenital anomalies and vascular birthmarks of the lower extremities. Magn Reson Imaging Clin N Am 1998 6 (3) 497-519
18. Gloviczki P, Stanson A W., Stickler G B. et al. Klippel-Trenaunay syndrome: the risks and benefits of vascular interventions. Surgery 1991 110 (3) 469-479
19. Eifert S, Villavicencio J L., Kao T C., Taute B M., Rich N M. Prevalence of deep venous anomalies in congenital vascular malformations of venous predominance. J Vasc Surg 2000 31 (3) 462-471
20. Capraro P A., Fisher J, Hammond D C., Grossman J A. Klippel-Trenaunay syndrome. Plast Reconstr Surg 2002 109 (6) 2052-2060 quiz 2061-2052 (Pubitemid 34492438)
21. Servelle M. Klippel and Trénaunay's syndrome. 768 operated cases. Ann Surg 1985 201 (3) 365-373
22. Alomari A I., Karian V E., Lord D J., Padua H M., Burrows P E. Percutaneous sclerotherapy for lymphatic malformations: a retrospective analysis of patient-evaluated improvement. J Vasc Interv Radiol 2006 17 (10) 1639-1648
23. Garzon M C., Huang J T., Enjolras O, Frieden I J. Vascular malformations: Part I. J Am Acad Dermatol 2007 56 (3) 353-370 quiz 371-354
24. Lee A, Driscoll D, Gloviczki P, Clay R, Shaughnessy W, Stans A. Evaluation and management of pain in patients with Klippel-Trenaunay syndrome: a review. Pediatrics 2005 115 (3) 744-749
25. Bird L M., Jones M C., Kuppermann N, Huskins W C. Gram-negative bacteremia in four patients with Klippel-Trenaunay-Weber syndrome. Pediatrics 1996 97 (5) 739-741
26. Neubert A G., Golden M A., Rose N C. Kasabach-Merritt coagulopathy complicating Klippel-Trenaunay-Weber syndrome in pregnancy. Obstet Gynecol 1995 85 (5 Pt 2) 831-833
27. Laor T, Hoffer F A., Burrows P E., Kozakewich H P. MR lymphangiography in infants, children, and young adults. AJR Am J Roentgenol 1998 171 (4) 1111-1117
28. Donnelly L F., Adams D M., Bisset G S. III. Vascular malformations and hemangiomas: a practical approach in a multidisciplinary clinic. AJR Am J Roentgenol 2000 174 (3) 597-608
29. Breugem C C., Maas M, Reekers J A., van der Horst C M. Use of magnetic resonance imaging for the evaluation of vascular malformations of the lower extremity. Plast Reconstr Surg 2001 108 (4) 870-877 (Pubitemid 32847706)
30. Hein K D., Mulliken J B., Kozakewich H P., Upton J, Burrows P E. Venous malformations of skeletal muscle. Plast Reconstr Surg 2002 110 (7) 1625-1635
31. Meyer J S., Hoffer F A., Barnes P D., Mulliken J B. Biological classification of soft-tissue vascular anomalies: MR correlation. AJR Am J Roentgenol 1991 157 (3) 559-564
32. Baskerville P A., Ackroyd J S., Browse N L. The etiology of the Klippel-Trenaunay syndrome. Ann Surg 1985 202 (5) 624-627
33. Enjolras O, Logeart I, Gelbert F et al. Arteriovenous malformations: a study of 200 cases [in French]. Ann Dermatol Venereol 2000 127 (1) 17-22
34. Mulliken J B., Young A E. In: Vascular Birthmarks: Hemangiomas and Vascular Malformations. Philadelphia, PA WB Saunders 1988
35. Ziyeh S, Spreer J, Rössler J et al. Parkes Weber or Klippel-Trenaunay syndrome? Non-invasive diagnosis with MR projection angiography. Eur Radiol 2004 14 (11) 2025-2029
36. White R I. Jr, Pollak J, Persing J, Henderson K J., Thomson J G., Burdge C M. Long-term outcome of embolotherapy and surgery for high-flow extremity arteriovenous malformations. J Vasc Interv Radiol 2000 11 (10) 1285-1295
37. Upton J, Coombs C J., Mulliken J B., Burrows P E., Pap S. Vascular malformations of the upper limb: a review of 270 patients. J Hand Surg [Am] 1999 24 (5) 1019-1035
38. van Rijswijk C S., van der Linden E, van der Woude H J., van Baalen J M., Bloem J L. Value of dynamic contrast-enhanced MR imaging in diagnosing and classifying peripheral vascular malformations. AJR Am J Roentgenol 2002 178 (5) 1181-1187
39. Dobson M J., Hartley R W., Ashleigh R, Watson Y, Hawnaur J M. MR angiography and MR imaging of symptomatic vascular malformations. Clin Radiol 1997 52 (8) 595-602
40. Siegel M J., Glazer H S., St Amour T E., Rosenthal D D. Lymphangiomas in children: MR imaging. Radiology 1989 170 (2) 467-470
41. Laor T, Burrows P E., Hoffer F A. Magnetic resonance venography of congenital vascular malformations of the extremities. Pediatr Radiol 1996 26 (6) 371-380
42. Rak K M., Yakes W F., Ray R L. et al. MR imaging of symptomatic peripheral vascular malformations. AJR Am J Roentgenol 1992 159 (1) 107-112
43. Roebuck D J. Klippel-Trénaunay and Parkes-Weber syndromes. AJR Am J Roentgenol 1997 169 (1) 311-312
44. Baskerville P A., Ackroyd J S., Lea Thomas M, Browse N L. The Klippel-Trenaunay syndrome: clinical, radiological and haemodynamic features and management. Br J Surg 1985 72 (3) 232-236
45. Mulliken J B., Young A E. Vascular Birthmarks: Hemangiomas and Malformations. Philadelphia, PA WB Saunders 1988
46. Claudon M, Upton J, Burrows P E. Diffuse venous malformations of the upper limb: morphologic characterization by MRI and venography. Pediatr Radiol 2001 31 (7) 507-514
47. Tan W H., Baris H N., Burrows P E. et al. The spectrum of vascular anomalies in patients with PTEN mutations: implications for diagnosis and management. J Med Genet 2007 44 (9) 594-602
48. Frieden I, Enjolras O, Esterly N. Vascular birthmarks and other abnormalities of blood vessels and lymphatics In: Schachner La, Hansen RC Pediatric dermatology. St. Louis, MO Mosby 2003 833-862
49. Hendriks Y M., Verhallen J T., van der Smagt J J. et al. Bannayan-Riley-Ruvalcaba syndrome: further delineation of the phenotype and management of PTEN mutation-positive cases. Fam Cancer 2003 2 (2) 79-85
50. Gorlin R J., Cohen M M. Jr, Condon L M., Burke B A. Bannayan-Riley- Ruvalcaba syndrome. Am J Med Genet 1992 44 (3) 307-314
51. Biesecker L. The challenges of Proteus syndrome: diagnosis and management. Eur J Hum Genet 2006 14 (11) 1151-1157
52. Elsayes K M., Menias C O., Dillman J R., Platt J F., Willatt J M., Heiken J P. Vascular malformation and hemangiomatosis syndromes: spectrum of imaging manifestations. AJR Am J Roentgenol 2008 190 (5) 1291-1299
53. Linton J A., Seo B K., Oh C S. Proteus syndrome: a natural clinical course of Proteus syndrome. Yonsei Med J 2002 43 (2) 259-266
54. Nguyen D, Turner J T., Olsen C, Biesecker L G., Darling T N. Cutaneous manifestations of proteus syndrome: correlations with general clinical severity. Arch Dermatol 2004 140 (8) 947-953
55. Twede J V., Turner J T., Biesecker L G., Darling T N. Evolution of skin lesions in Proteus syndrome. J Am Acad Dermatol 2005 52 (5) 834-838
56. Wiedemann H R., Burgio G R., Aldenhoff P, Kunze J, Kaufmann H J., Schirg E. The proteus syndrome. Partial gigantism of the hands and/or feet, nevi, hemihypertrophy, subcutaneous tumors, macrocephaly or other skull anomalies and possible accelerated growth and visceral affections. Eur J Pediatr 1983 140 (1) 5-12
57. Eberhard D A. Two-year-old boy with Proteus syndrome and fatal pulmonary thromboembolism. Pediatr Pathol 1994 14 (5) 771-779
58. Slavotinek A M., Vacha S J., Peters K F., Biesecker L G. Sudden death caused by pulmonary thromboembolism in Proteus syndrome. Clin Genet 2000 58 (5) 386-389
59. Cohen M M. Jr. Causes of premature death in Proteus syndrome. Am J Med Genet 2001 101 (1) 1-3
60. del Boz González J, Serrano Martín M M., Vera Casaño A. [Cutis marmorata telangiectatica congenita. Review of 33 cases [in Spanish]. An Pediatr (Barc) 2008 69 (6) 557-564
61. Kienast A K., Hoeger P H. Cutis marmorata telangiectatica congenita: a prospective study of 27 cases and review of the literature with proposal of diagnostic criteria. Clin Exp Dermatol 2009 34 (3) 319-323
62. McDermott A L., Dutt S N., Chavda S V., Morgan D W. Maffucci's syndrome: clinical and radiological features of a rare condition. J Laryngol Otol 2001 115 (10) 845-847
63. Requena L, Sangueza O P. Cutaneous vascular anomalies. Part I. Hamartomas, malformations, and dilation of preexisting vessels. J Am Acad Dermatol 1997 37 (4) 523-549 quiz 549-552
64. Hisaoka M, Aoki T, Kouho H, Chosa H, Hashimoto H. Maffucci's syndrome associated with spindle cell hemangioendothelioma. Skeletal Radiol 1997 26 (3) 191-194
65. Garzon M C., Enjolras O, Frieden I J. Vascular tumors and vascular malformations: evidence for an association. J Am Acad Dermatol 2000 42 (2 Pt 1) 275-279
66. Schwartz H S., Zimmerman N B., Simon M A., Wroble R R., Millar E A., Bonfiglio M. The malignant potential of enchondromatosis. J Bone Joint Surg Am 1987 69 (2) 269-274
67. Lee N H., Choi E H., Choi W K., Lee S H., Ahn S K. Maffucci's syndrome with oral and intestinal haemangioma. Br J Dermatol 1999 140 (5) 968-969
68. Auyeung J, Mohanty K, Tayton K. Maffucci lymphangioma syndrome: an unusual variant of Ollier's disease, a case report and a review of the literature. J Pediatr Orthop B 2003 12 (2) 147-150
69. Murphey M D., Fairbairn K J., Parman L M., Baxter K G., Parsa M B., Smith W S. From the archives of the AFIP. Musculoskeletal angiomatous lesions: radiologic-pathologic correlation. Radiographics 1995 15 (4) 893-917
70. Albregts A E., Rapini R P. Malignancy in Maffucci's syndrome. Dermatol Clin 1995 13 (1) 73-78
71. Zwenneke Flach H, Ginai A Z., Wolter Oosterhuis J, Armed Forces Institutes of Pathology. Best cases from the AFIP. Maffucci syndrome: radiologic and pathologic findings. Radiographics 2001 21 (5) 1311-1316
72. Newland L, Kong K, Gallagher R, Turner J. Disappearing bones: a case of Gorham-Stout disease. Pathology 2008 40 (4) 420-423
73. Bruch-Gerharz D, Gerharz C D., Stege H et al. Cutaneous lymphatic malformations in disappearing bone (Gorham-Stout) disease: a novel clue to the pathogenesis of a rare syndrome. J Am Acad Dermatol 2007 56 (2, Suppl) S21-S25
74. Stavlas P, Katsiva V, Kouvaras Y. Massive osteolysis of the hip: Gorham's disease. Orthopedics 2007 30 (12) 1059-1060
75. Schumann E, Wild A, Seller K. Gorham-stout disease [in German]. Z Orthop Unfall 2008 146 (5) 655-659
76. Radhakrishnan K, Rockson S G. Gorham's disease: an osseous disease of lymphangiogenesis? Ann N Y Acad Sci 2008 1131 203-205
77. Malik R, Malik R, Tandon S, Tandon P. Skeletal angiomatosisrare cause of bone destruction: a case report with review of literature. Indian J Pathol Microbiol 2008 51 (4) 515-518
78. Escande C, Schouman T, Françoise G et al. Histological features and management of a mandibular Gorham disease: a case report and review of maxillofacial cases in the literature. Oral Surg Oral Med Oral Pathol Oral Radiol Endod 2008 106 (3) e30-e37
79. Chong Ng L, Sell P. Gorham disease of the cervical spinea case report and review of the literature. Spine (Phila Pa 1976) 2003 28 (18) E355-E358
80. Assoun J, Richardi G, Railhac J J. et al. CT and MRI of massive osteolysis of Gorham. J Comput Assist Tomogr 1994 18 (6) 981-984
81. Patel D V. Gorham's disease or massive osteolysis. Clin Med Res 2005 3 (2) 65-74
82. Hirayama T, Sabokbar A, Itonaga I, Watt-Smith S, Athanasou N A. Cellular and humoral mechanisms of osteoclast formation and bone resorption in Gorham-Stout disease. J Pathol 2001 195 (5) 624-630
83. Gorham L W., Stout A P. Massive osteolysis (acute spontaneous absorption of bone, phantom bone, disappearing bone); its relation to hemangiomatosis. J Bone Joint Surg Am 1955 37-A (5) 985-1004
84. Heyden G, Kindblom L G., Nielsen J M. Disappearing bone disease. A clinical and histological study. J Bone Joint Surg Am 1977 59 (1) 57-61
85. Cannon S R. Massive osteolysis. A review of seven cases. J Bone Joint Surg Br 1986 68 (1) 24-28
86. Pedicelli G, Mattia P, Zorzoli A A., Sorrone A, De Martino F, Sciotto V. Gorham syndrome. JAMA 1984 252 (11) 1449-1451
87. Halliday D R., Dahlin D C., Pugh D G., Young H H. Massive osteolysis and angiomatosis. Radiology 1964 82 637-644
88. Drewry G R., Sutterlin C E. III, Martinez C R., Brantley S G. Gorham disease of the spine. Spine (Phila Pa 1976) 1994 19 (19) 2213-2222
89. Hagendoorn J, Padera T P., Yock T I. et al. Platelet-derived growth factor receptor-beta in Gorham's disease. Nat Clin Pract Oncol 2006 3 (12) 693-697
90. Yildiz T S., Kus A, Solak M, Toker K. The Gorham-Stout syndrome: one lung ventilation with a bronchial blocker. A case of Gorham's disease with chylothorax. Paediatr Anaesth 2009 19 (2) 190-191
91. Kose M, Pekcan S, Dogru D et al. Gorham-Stout syndrome with chylothorax: successful remission by interferon alpha-2b. Pediatr Pulmonol 2009 44 (6) 613-615
92. Boyle M J., Alison P, Taylor G, Lightbourne B A. A case of Gorham's disease complicated by bilateral chylothorax. Heart Lung Circ 2008 17 (1) 64-66
93. Bernstein J, Engelhardt M, Retzlaff S. A rare differential diagnosis of chylothorax [in German]. Pneumologie 2008 62 (4) 196-199
94. Atalabi O M., Fishman S J., Kozakewich H P., Alsamarah A Y., Alomari A I. A lethal form of Gorham disease associated with extensive musculoskeletal pneumatosis: case report and review of the literature. Skeletal Radiol 2008 37 (11) 1041-1046
95. Fisher K L., Pogrel M A. Gorham's syndrome (massive osteolysis): a case report. J Oral Maxillofac Surg 1990 48 (11) 1222-1225
96. Vinée P, Tanyü M O., Hauenstein K H., Sigmund G, Stöver B, Adler C P. CT and MRI of Gorham syndrome. J Comput Assist Tomogr 1994 18 (6) 985-989
97. Möller G, Priemel M, Amling M, Werner M, Kuhlmey A S., Delling G. The Gorham-Stout syndrome (Gorham's massive osteolysis). A report of six cases with histopathological findings. J Bone Joint Surg Br 1999 81 (3) 501-506
98. Mendez A A., Keret D, Robertson W, MacEwen G D. Massive osteolysis of the femur (Gorham's disease): a case report and review of the literature. J Pediatr Orthop 1989 9 (5) 604-608
99. Tie M L., Poland G A., Rosenow E C. III. Chylothorax in Gorham's syndrome. A common complication of a rare disease. Chest 1994 105 (1) 208-213
100. Fujiu K, Kanno R, Suzuki H, Nakamura N, Gotoh M. Chylothorax associated with massive osteolysis (Gorham's syndrome). Ann Thorac Surg 2002 73 (6) 1956-1957
101. Kery L, Wouters H W. Massive osteolysis. Report of two cases. J Bone Joint Surg Br 1970 52 (3) 452-459
102. Berkley E M., Gill G J., Moore L E., Rayburn W F. Consumptive coagulopathy associated with Gorham syndrome and subsequent Kasabach-Merritt syndrome during pregnancy: a case report. J Reprod Med 2007 52 (12) 1103-1106
103. Kerhoas Nicolas C K., Le Bidaut M, Dosquet C, Enjolras O, Stalder J F. Kasabach-Merritt syndrome of the leg associated with osteolysis or Gorham sign [in French]. Ann Dermatol Venereol 1997 124 (12) 852-854
104. Heffez L, Doku H C., Carter B L., Feeney J E. Perspectives on massive osteolysis. Report of a case and review of the literature. Oral Surg Oral Med Oral Pathol 1983 55 (4) 331-343
105. Choma N D., Biscotti C V., Bauer T W., Mehta A C., Licata A A. Gorham's syndrome: a case report and review of the literature. Am J Med 1987 83 (6) 1151-1156
106. Auge B, Toussirot E, Kantelip B, Wendling D. From polycystic bone angiomatosis to Gorham's disease. Two case-reports and literature review. Rev Rhum Engl Ed 1998 65 (3) 201-206
107. Chung C, Yu J S., Resnick D, Vaughan L M., Haghighi P. Gorham syndrome of the thorax and cervical spine: CT and MRI findings. Skeletal Radiol 1997 26 (1) 55-59
108. Yoo S Y., Hong S H., Chung H W., Choi J A., Kim C J., Kang H S. MRI of Gorham's disease: findings in two cases. Skeletal Radiol 2002 31 (5) 301-306
109. Yalniz E, Alicioglu B, Benlier E, Yilmaz B, Altaner S. Gorham-Stout disease of the humerus. JBR-BTR 2008 91 (1) 14-17
110. Spieth M E., Greenspan A, Forrester D M., Ansari A N., Kimura R L., Gleason-Jordan I. Gorham's disease of the radius: radiographic, scintigraphic, and MRI findings with pathologic correlation. A case report and review of the literature. Skeletal Radiol 1997 26 (11) 659-663
111. Kai B, Ryan A, Munk P L., Dunlop P. Gorham disease of bone: three cases and review of radiological features. Clin Radiol 2006 61 (12) 1058-1064
112. Liu N F., Wang C G. The role of magnetic resonance imaging in diagnosis of peripheral lymphatic disorders. Lymphology 1998 31 (3) 119-127
113. Dominguez R, Washowich T L. Gorham's disease or vanishing bone disease: plain film, CT, and MRI findings of two cases. Pediatr Radiol 1994 24 (5) 316-318
114. Bullough P G. Massive osteolysis. N Y State J Med 1971 71 (19) 2267-2278
115. Nixon G W. Lymphangiomatosis of bone demonstrated by lymphangiography. Am J Roentgenol Radium Ther Nucl Med 1970 110 (3) 582-586
116. Tsyb A F., Mukhamedzhanov I K., Guseva L I. Lymphangiomatosis of bone and soft tissue (results of lymphangiographic examinations). Lymphology 1983 16 (3) 181-184
117. Campbell J, Almond H G., Johnson R. Massive osteolysis of the humerus with spontaneous recovery. J Bone Joint Surg Br 1975 57 (2) 238-240
118. Hagberg H, Lamberg K, Aström G. Alpha-2b interferon and oral clodronate for Gorham's disease. Lancet 1997 350 (9094) 1822-1823
119. Schultz K, Rosenberg A E., Ebb D H., Mankin H J. Lower-extremity lymphangiomatosis. A case report with a seventeen-year follow-up. J Bone Joint Surg Am 2005 87 (1) 162-167
120. Hanly J G., Walsh N M., Bresnihan B. Massive osteolysis in the hand and response to radiotherapy. J Rheumatol 1985 12 (3) 580-582
121. Dunbar S F., Rosenberg A, Mankin H, Rosenthal D, Suit H D. Gorham's massive osteolysis: the role of radiation therapy and a review of the literature. Int J Radiat Oncol Biol Phys 1993 26 (3) 491-497
122. Shives T C., Beabout J W., Unni K K. Massive osteolysis. Clin Orthop Relat Res 1993 (294) 267-276