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Erschienen in: Japanese Journal of Radiology 10/2017

09.08.2017 | Original Article

MR imaging findings of vertebral involvement in Gorham–Stout disease, generalized lymphatic anomaly, and kaposiform lymphangiomatosis

verfasst von: Hiroki Kato, Michio Ozeki, Toshiyuki Fukao, Masayuki Matsuo

Erschienen in: Japanese Journal of Radiology | Ausgabe 10/2017

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Abstract

Purpose

To assess the MR imaging findings of vertebral involvement in Gorham–Stout disease (GSD), generalized lymphatic anomaly (GLA), and kaposiform lymphangiomatosis (KLA).

Methods

Nine patients (three patients with GSD, three with GLA, and three with KLA) who underwent whole-spine MR examinations were included. MR findings of fatty marrow replacement and prolonged T1 and T2 lesions of the vertebrae were retrospectively assessed. Prolonged T1 and T2 lesions were defined as well-defined and round-, oval-, or geographic-shaped areas.

Results

Six patients [one (33%) patient with GSD, two (67%) with GLA, and three (100%) with KLA] showed both fatty marrow replacement and prolonged T1 and T2 lesions. Fatty marrow replacement was seen in the cervical spine of two (33%) patients, thoracic spine of six (100%), lumbar spine of six (100%), and sacral spine of two (33%). Prolonged T1 and T2 lesions were seen in the cervical spine of three (50%) patients, thoracic spine of three (50%), lumbar spine of six (100%), and sacral spine of three (50%).

Conclusion

Both fatty marrow replacement and prolonged T1 and T2 lesions of the vertebrae could be observed in GSD, GLA, and KLA. The most commonly affected site was the lumbar spine, followed by the thoracic spine.
Literatur
1.
Zurück zum Zitat 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:e203–14.CrossRefPubMed 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:e203–14.CrossRefPubMed
2.
Zurück zum Zitat Gorham LW, Wright AW, Shultz HH, Maxon FC Jr. Disappearing bones: a rare form of massive osteolysis; report of two cases, one with autopsy findings. Am J Med. 1954;17:674–82.CrossRefPubMed Gorham LW, Wright AW, Shultz HH, Maxon FC Jr. Disappearing bones: a rare form of massive osteolysis; report of two cases, one with autopsy findings. Am J Med. 1954;17:674–82.CrossRefPubMed
3.
Zurück zum Zitat Gorham LW, Stout AP. Massive osteolysis (acute spontaneous absorption of bone, phantom bone, disappearing bone); its relation to hemangiomatosis. J Bone Jt Surg Am. 1955;37-A:985–1004.CrossRef Gorham LW, Stout AP. Massive osteolysis (acute spontaneous absorption of bone, phantom bone, disappearing bone); its relation to hemangiomatosis. J Bone Jt Surg Am. 1955;37-A:985–1004.CrossRef
4.
Zurück zum Zitat Johnson PM, Mc CJ. Observations on massive osteolysis; a review of the literature and report of a case. Radiology. 1958;71:28–42.CrossRefPubMed Johnson PM, Mc CJ. Observations on massive osteolysis; a review of the literature and report of a case. Radiology. 1958;71:28–42.CrossRefPubMed
5.
Zurück zum Zitat Pastakia B, Horvath K, Lack EE. Seventeen-year follow-up and autopsy findings in a case of massive osteolysis. Skelet Radiol. 1987;16:291–7.CrossRef Pastakia B, Horvath K, Lack EE. Seventeen-year follow-up and autopsy findings in a case of massive osteolysis. Skelet Radiol. 1987;16:291–7.CrossRef
6.
Zurück zum Zitat Radhakrishnan K, Rockson SG. Gorham’s disease: an osseous disease of lymphangiogenesis? Ann N Y Acad Sci. 2008;1131:203–5.CrossRefPubMed Radhakrishnan K, Rockson SG. Gorham’s disease: an osseous disease of lymphangiogenesis? Ann N Y Acad Sci. 2008;1131:203–5.CrossRefPubMed
7.
Zurück zum Zitat Dellinger MT, Garg N, Olsen BR. Viewpoints on vessels and vanishing bones in Gorham–Stout disease. Bone. 2014;63:47–52.CrossRefPubMed Dellinger MT, Garg N, Olsen BR. Viewpoints on vessels and vanishing bones in Gorham–Stout disease. Bone. 2014;63:47–52.CrossRefPubMed
8.
Zurück zum Zitat Rossler J, Saueressig U, Kayser G, von Winterfeld M, Klement GL. Personalized therapy for generalized lymphatic anomaly/Gorham–Stout disease with a combination of sunitinib and taxol. J Pediatr Hematol Oncol. 2015;37:e481–5.CrossRefPubMedPubMedCentral Rossler J, Saueressig U, Kayser G, von Winterfeld M, Klement GL. Personalized therapy for generalized lymphatic anomaly/Gorham–Stout disease with a combination of sunitinib and taxol. J Pediatr Hematol Oncol. 2015;37:e481–5.CrossRefPubMedPubMedCentral
9.
Zurück zum Zitat Alvarez OA, Kjellin I, Zuppan CW. Thoracic lymphangiomatosis in a child. J Pediatr Hematol Oncol. 2004;26:136–41.CrossRefPubMed Alvarez OA, Kjellin I, Zuppan CW. Thoracic lymphangiomatosis in a child. J Pediatr Hematol Oncol. 2004;26:136–41.CrossRefPubMed
10.
Zurück zum Zitat Croteau SE, Kozakewich HP, Perez-Atayde AR, Fishman SJ, Alomari AI, Chaudry G, et al. Kaposiform lymphangiomatosis: a distinct aggressive lymphatic anomaly. J Pediatr. 2014;164:383–8.CrossRefPubMed Croteau SE, Kozakewich HP, Perez-Atayde AR, Fishman SJ, Alomari AI, Chaudry G, et al. Kaposiform lymphangiomatosis: a distinct aggressive lymphatic anomaly. J Pediatr. 2014;164:383–8.CrossRefPubMed
11.
Zurück zum Zitat Goyal P, Alomari AI, Kozakewich HP, Trenor CC 3rd, Perez-Atayde AR, Fishman SJ, et al. Imaging features of kaposiform lymphangiomatosis. Pediatr Radiol. 2016;46:1282–90.CrossRefPubMed Goyal P, Alomari AI, Kozakewich HP, Trenor CC 3rd, Perez-Atayde AR, Fishman SJ, et al. Imaging features of kaposiform lymphangiomatosis. Pediatr Radiol. 2016;46:1282–90.CrossRefPubMed
12.
Zurück zum Zitat Ozeki M, Fujino A, Matsuoka K, Nosaka S, Kuroda T, Fukao T. Clinical features and prognosis of generalized lymphatic anomaly, kaposiform lymphangiomatosis, and Gorham–Stout disease. Pediatr Blood Cancer. 2016;63:832–8.CrossRefPubMed Ozeki M, Fujino A, Matsuoka K, Nosaka S, Kuroda T, Fukao T. Clinical features and prognosis of generalized lymphatic anomaly, kaposiform lymphangiomatosis, and Gorham–Stout disease. Pediatr Blood Cancer. 2016;63:832–8.CrossRefPubMed
13.
Zurück zum Zitat Lala S, Mulliken JB, Alomari AI, Fishman SJ, Kozakewich HP, Chaudry G. Gorham–Stout disease and generalized lymphatic anomaly–clinical, radiologic, and histologic differentiation. Skelet Radiol. 2013;42:917–24.CrossRef Lala S, Mulliken JB, Alomari AI, Fishman SJ, Kozakewich HP, Chaudry G. Gorham–Stout disease and generalized lymphatic anomaly–clinical, radiologic, and histologic differentiation. Skelet Radiol. 2013;42:917–24.CrossRef
14.
Zurück zum Zitat Bode-Lesniewska B, von Hochstetter A, Exner GU, Hodler J. Gorham–Stout disease of the shoulder girdle and cervico-thoracic spine: fatal course in a 65-year-old woman. Skelet Radiol. 2002;31:724–9.CrossRef Bode-Lesniewska B, von Hochstetter A, Exner GU, Hodler J. Gorham–Stout disease of the shoulder girdle and cervico-thoracic spine: fatal course in a 65-year-old woman. Skelet Radiol. 2002;31:724–9.CrossRef
15.
Zurück zum Zitat Ceroni D, De Coulon G, Regusci M, Kaelin A. Gorham–Stout disease of costo-vertebral localization: radiographic, scintigraphic, computed tomography, and magnetic resonance imaging findings. Acta Radiol. 2004;45:464–8.CrossRefPubMed Ceroni D, De Coulon G, Regusci M, Kaelin A. Gorham–Stout disease of costo-vertebral localization: radiographic, scintigraphic, computed tomography, and magnetic resonance imaging findings. Acta Radiol. 2004;45:464–8.CrossRefPubMed
16.
Zurück zum Zitat Dominguez R, Washowich TL. Gorham’s disease or vanishing bone disease: plain film, CT, and MRI findings of two cases. Pediatr Radiol. 1994;24:316–8.CrossRefPubMed Dominguez R, Washowich TL. Gorham’s disease or vanishing bone disease: plain film, CT, and MRI findings of two cases. Pediatr Radiol. 1994;24:316–8.CrossRefPubMed
17.
Zurück zum Zitat Livesley PJ, Saifuddin A, Webb PJ, Mitchell N, Ramani P. Gorham’s disease of the spine. Skelet Radiol. 1996;25:403–5.CrossRef Livesley PJ, Saifuddin A, Webb PJ, Mitchell N, Ramani P. Gorham’s disease of the spine. Skelet Radiol. 1996;25:403–5.CrossRef
18.
Zurück zum Zitat Safi F, Gupta A, Adams D, Anandan V, McCormack FX, Assaly R. Kaposiform lymphangiomatosis, a newly characterized vascular anomaly presenting with hemoptysis in an adult woman. Ann Am Thorac Soc. 2014;11:92–5.CrossRefPubMed Safi F, Gupta A, Adams D, Anandan V, McCormack FX, Assaly R. Kaposiform lymphangiomatosis, a newly characterized vascular anomaly presenting with hemoptysis in an adult woman. Ann Am Thorac Soc. 2014;11:92–5.CrossRefPubMed
19.
Zurück zum Zitat Luks VL, Kamitaki N, Vivero MP, Uller W, Rab R, Bovee JV, et al. Lymphatic and other vascular malformative/overgrowth disorders are caused by somatic mutations in PIK3CA. J Pediatr. 2015;166(1048–54):e1–5. Luks VL, Kamitaki N, Vivero MP, Uller W, Rab R, Bovee JV, et al. Lymphatic and other vascular malformative/overgrowth disorders are caused by somatic mutations in PIK3CA. J Pediatr. 2015;166(1048–54):e1–5.
20.
21.
Zurück zum Zitat Adams DM, Trenor CC 3rd, Hammill AM, Vinks AA, Patel MN, Chaudry G, et al. Efficacy and safety of sirolimus in the treatment of complicated vascular anomalies. Pediatrics. 2016;137:e20153257.CrossRefPubMedPubMedCentral Adams DM, Trenor CC 3rd, Hammill AM, Vinks AA, Patel MN, Chaudry G, et al. Efficacy and safety of sirolimus in the treatment of complicated vascular anomalies. Pediatrics. 2016;137:e20153257.CrossRefPubMedPubMedCentral
23.
Zurück zum Zitat Shah LM, Hanrahan CJ. MRI of spinal bone marrow: Part I. Techniques and normal age-related appearances. AJR Am J Roentgenol. 2011;197:1298–308.CrossRefPubMed Shah LM, Hanrahan CJ. MRI of spinal bone marrow: Part I. Techniques and normal age-related appearances. AJR Am J Roentgenol. 2011;197:1298–308.CrossRefPubMed
24.
Zurück zum Zitat Hanrahan CJ, Shah LM. MRI of spinal bone marrow: Part 2. T1-weighted imaging-based differential diagnosis. AJR Am J Roentgenol. 2011;197:1309–21.CrossRefPubMed Hanrahan CJ, Shah LM. MRI of spinal bone marrow: Part 2. T1-weighted imaging-based differential diagnosis. AJR Am J Roentgenol. 2011;197:1309–21.CrossRefPubMed
Metadaten
Titel
MR imaging findings of vertebral involvement in Gorham–Stout disease, generalized lymphatic anomaly, and kaposiform lymphangiomatosis
verfasst von
Hiroki Kato
Michio Ozeki
Toshiyuki Fukao
Masayuki Matsuo
Publikationsdatum
09.08.2017
Verlag
Springer Japan
Erschienen in
Japanese Journal of Radiology / Ausgabe 10/2017
Print ISSN: 1867-1071
Elektronische ISSN: 1867-108X
DOI
https://doi.org/10.1007/s11604-017-0674-3

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