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Sturge-Weber and Klippel-Trenaunay Syndrome With Nevus of Ota and Ito

Sturge-Weber and Klippel-Trenaunay Syndrome With Nevus of Ota and Ito Abstract The patient was a 25-year-old Japanese woman with an extensive nevus flammeus which extended primarily over the left side of her face and the right side of the trunk and extremities. She had been blind in the left eye since birth. A bluish macular discoloration was noted over both sides of the face (nevus of Ota) and the right shoulder (nevus of Ito). Muscle strength of the right extremities was remarkably diminished and the right extremities were longer than the left. Results of radiological examination of the skull showed a remarkable hypertrophy of the bones of the ipsilateral side of the nevus flammeus. The combination of Sturge-Weber and Klippel-Trénaunay syndromes indicates a nosological relationship. References 1. Schirmer RS: Ein Fall von Telangiektasie . Graefe Arch Ophthal 7:119-121, 1860. 2. Sturge WA: A case of partial epilepsy due to a lesion of one of the vasomotor centres of the brain . Trans Clin Soc London 12:162-167, 1879. 3. Volland R: Über zwei Fäller von zerebralem Angiom nebst Bemerkungen über Hirnangiome . Z Erforsch Behandl Jugendl Schwachsinns 6:130-150, 1912. 4. Hebold O: Hämagiom der weichen Hirnhaut bei Naevus Vascularis des Gesichts . Arch Psychiat Nervenkr 51:445-456, 1913.Crossref 5. Dimitri V: Tumor cerebral congenito (angioma cavernosum) . Rev Assoc Méd Argent 36:1029-1037, 1923. 6. Weber FP: Right-sided hemi-hypotrophy resulting from right-sided congenital spastic hemiplegia, with a morbid condition of the left side of the brain, revealed by radiograms . J Neurol Psychopath 3:134-139, 1922.Crossref 7. Weber FP: A note on the association of extensive haemangiomatous naevus of skin with cerebral (meningeal) hemangioma, especially cases of facial vascular naevus with contralateral hemiplegia . Proc Roy Soc Med 22:431-442, 1929. 8. Krabbe K: Recherches anatomopathologiques sur un cas de soidisant angiome calcifié des méninges démontré par la radiographie . Rev Neurol 1:1394-1397, 1932. 9. Krabbe K: Facial and meningeal angiomatosis associated with calcifications of the brain cortex . Arch Neurol Psychiat 32:737-755, 1934.Crossref 10. Bergstrand H: On the classification of the haemangiomatous tumours and malformations of the central nervous system . Acta Path Microbiol 26 (suppl) :89-95, 1936. 11. Klippel M, Trénaunay P: Du naevus variqueux ostéo-hypertrophique . Arch Gen Med 3:641-672, 1900. 12. Weber FP: Angioma formation in connection with hypertrophy of limbs and hemi-hypertrophy . Brit J Derm 19:231-235, 1907. 13. Weber FP: Hemangiectatic hypertrophy of limbs: Congenital phlebarteriectasia and so-called congenital varicose veins . Brit J Child Dis 15:13-17, 1918. 14. Lindenauer SM: The Klippel-Trénaunay syndrome: Varicosity, hypertrophy and hemangioma with no arteriovenous fistula . Ann Surg 162:303-314, 1965.Crossref 15. Mullins JF, Naylor D, Redetski J: The Klippel-Trénaunay-Weber syndrome . Arch Derm 86:202-206, 1962.Crossref 16. Tanino H: Über eine in Japan häufig vorkommende Nävusform: "Naevus Fusco-caeruleus ophthalmo-maxillaris Ota." I. Mitteilung: Beobachtung über Lokalisation, Verfärbung, Anordnung und histologische Veränderung . Jap J Derm 46:107-111, 1939. 17. Kopf AW, Weidman AI: Nevus of Ota . Arch Derm 85:195-208, 1962.Crossref 18. Ito M: Nevus fusco-caeruleus acromio-deltoideus . Tohoku J Exp Med 60:10, 1954.Crossref 19. Riehm H, Dressler F, Bachmann D: Klippel-Trénaunay-Weber-Syndrom-Weber-Syndrom und Trisomie 21 bei zwei Jugendlichen . Mschr Kinderheilk 116:24-28, 1968. 20. Hayward MD, Bower BD: Chromosomal trisomy associated with the Sturge-Weber syndrome . Lancet 2:844-846, 1960.Crossref 21. Patau K, Therman E, Smith DW, et al: Partial trisomy syndromes: I. Sturge-Weber's disease . Amer J Hum Genet 13:287-298, 1961. 22. Lindgren E: Über corticale Verkalkungen im Gehirn . Nervenarzt 12:138-142, 1939. 23. Zweimuller E: Das Krankheitsbild von Sturge-Weber-West . Osterr Z Kinderheilk 7:35-66, 1952. 24. Parnitzke KH: Symptomwert und Symptomverteilung bei der Sturge-Weberschen Krankheit. Zbl Neurochir 16:92-109, 1956. 25. Alexander GL, Norman RM: The Sturge-Weber Syndrome . Bristol, England, John Wright & Sons Ltd, 1960. 26. Strobel H: Die Sturge-Webersche Erkrankung und ihre Beziehungen zu anderen Syndromen . Arch Derm 183:468-482, 1943.Crossref 27. Furtado, cited by Rademacher.30 28. Teller H, Lindner B: Über Mischformen der Phakomatösen Syndrome von Sturge-Weber und Klippel-Trénaunay . Z Haut Geschlechtskr 13:113-120, 1952. 29. Koch G: Zur Klinik, Symptomatologie, Pathogenese und Erbpathologie des Klippel-Trénaunay-Weberschen Syndroms . Acta Genet Med Gemel 5( (suppl 1) ):326-370, 1952. 30. Rademacher R: Über einen Fall einer Kombination von Sturge-Weber und Klippel-Trénaunay Syndrom mit konstitutioneller Neurodermitis . Derm Wschr 143:381-384, 1961. 31. Kramer W: Syndromes of Klippel-Trénaunay and Sturge-Weber in the same patient . Psychiat Neurol Neurochir 66:362-370, 1963. 32. Lindgren E: Über corticale Verkalkungen im Gehirn. Nervenarzt 12:138-142, 1939. 33. Schnyder UW, Landolt E, Martz G: Syndrome de Klippel-Trénaunay avec colobome irien atypique . J Genet Hum 5:1-8, 1956. 34. Peters G: Sturge-Webersche Krankheit . Henke-Lubarsch-Rössle Handbuch der spezifische pathologische Anatomie und Histologie . Berlin, Springer-Verlag, 1958, vol 8, p 696. http://www.deepdyve.com/assets/images/DeepDyve-Logo-lg.png Archives of Dermatology American Medical Association

Sturge-Weber and Klippel-Trenaunay Syndrome With Nevus of Ota and Ito

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Publisher
American Medical Association
Copyright
Copyright © 1970 American Medical Association. All Rights Reserved.
ISSN
0003-987X
eISSN
1538-3652
DOI
10.1001/archderm.1970.04000120058010
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Abstract

Abstract The patient was a 25-year-old Japanese woman with an extensive nevus flammeus which extended primarily over the left side of her face and the right side of the trunk and extremities. She had been blind in the left eye since birth. A bluish macular discoloration was noted over both sides of the face (nevus of Ota) and the right shoulder (nevus of Ito). Muscle strength of the right extremities was remarkably diminished and the right extremities were longer than the left. Results of radiological examination of the skull showed a remarkable hypertrophy of the bones of the ipsilateral side of the nevus flammeus. The combination of Sturge-Weber and Klippel-Trénaunay syndromes indicates a nosological relationship. References 1. Schirmer RS: Ein Fall von Telangiektasie . Graefe Arch Ophthal 7:119-121, 1860. 2. Sturge WA: A case of partial epilepsy due to a lesion of one of the vasomotor centres of the brain . Trans Clin Soc London 12:162-167, 1879. 3. Volland R: Über zwei Fäller von zerebralem Angiom nebst Bemerkungen über Hirnangiome . Z Erforsch Behandl Jugendl Schwachsinns 6:130-150, 1912. 4. Hebold O: Hämagiom der weichen Hirnhaut bei Naevus Vascularis des Gesichts . Arch Psychiat Nervenkr 51:445-456, 1913.Crossref 5. Dimitri V: Tumor cerebral congenito (angioma cavernosum) . Rev Assoc Méd Argent 36:1029-1037, 1923. 6. Weber FP: Right-sided hemi-hypotrophy resulting from right-sided congenital spastic hemiplegia, with a morbid condition of the left side of the brain, revealed by radiograms . J Neurol Psychopath 3:134-139, 1922.Crossref 7. Weber FP: A note on the association of extensive haemangiomatous naevus of skin with cerebral (meningeal) hemangioma, especially cases of facial vascular naevus with contralateral hemiplegia . Proc Roy Soc Med 22:431-442, 1929. 8. Krabbe K: Recherches anatomopathologiques sur un cas de soidisant angiome calcifié des méninges démontré par la radiographie . Rev Neurol 1:1394-1397, 1932. 9. Krabbe K: Facial and meningeal angiomatosis associated with calcifications of the brain cortex . Arch Neurol Psychiat 32:737-755, 1934.Crossref 10. Bergstrand H: On the classification of the haemangiomatous tumours and malformations of the central nervous system . Acta Path Microbiol 26 (suppl) :89-95, 1936. 11. Klippel M, Trénaunay P: Du naevus variqueux ostéo-hypertrophique . Arch Gen Med 3:641-672, 1900. 12. Weber FP: Angioma formation in connection with hypertrophy of limbs and hemi-hypertrophy . Brit J Derm 19:231-235, 1907. 13. Weber FP: Hemangiectatic hypertrophy of limbs: Congenital phlebarteriectasia and so-called congenital varicose veins . Brit J Child Dis 15:13-17, 1918. 14. Lindenauer SM: The Klippel-Trénaunay syndrome: Varicosity, hypertrophy and hemangioma with no arteriovenous fistula . Ann Surg 162:303-314, 1965.Crossref 15. Mullins JF, Naylor D, Redetski J: The Klippel-Trénaunay-Weber syndrome . Arch Derm 86:202-206, 1962.Crossref 16. Tanino H: Über eine in Japan häufig vorkommende Nävusform: "Naevus Fusco-caeruleus ophthalmo-maxillaris Ota." I. Mitteilung: Beobachtung über Lokalisation, Verfärbung, Anordnung und histologische Veränderung . Jap J Derm 46:107-111, 1939. 17. Kopf AW, Weidman AI: Nevus of Ota . Arch Derm 85:195-208, 1962.Crossref 18. Ito M: Nevus fusco-caeruleus acromio-deltoideus . Tohoku J Exp Med 60:10, 1954.Crossref 19. Riehm H, Dressler F, Bachmann D: Klippel-Trénaunay-Weber-Syndrom-Weber-Syndrom und Trisomie 21 bei zwei Jugendlichen . Mschr Kinderheilk 116:24-28, 1968. 20. Hayward MD, Bower BD: Chromosomal trisomy associated with the Sturge-Weber syndrome . Lancet 2:844-846, 1960.Crossref 21. Patau K, Therman E, Smith DW, et al: Partial trisomy syndromes: I. Sturge-Weber's disease . Amer J Hum Genet 13:287-298, 1961. 22. Lindgren E: Über corticale Verkalkungen im Gehirn . Nervenarzt 12:138-142, 1939. 23. Zweimuller E: Das Krankheitsbild von Sturge-Weber-West . Osterr Z Kinderheilk 7:35-66, 1952. 24. Parnitzke KH: Symptomwert und Symptomverteilung bei der Sturge-Weberschen Krankheit. Zbl Neurochir 16:92-109, 1956. 25. Alexander GL, Norman RM: The Sturge-Weber Syndrome . Bristol, England, John Wright & Sons Ltd, 1960. 26. Strobel H: Die Sturge-Webersche Erkrankung und ihre Beziehungen zu anderen Syndromen . Arch Derm 183:468-482, 1943.Crossref 27. Furtado, cited by Rademacher.30 28. Teller H, Lindner B: Über Mischformen der Phakomatösen Syndrome von Sturge-Weber und Klippel-Trénaunay . Z Haut Geschlechtskr 13:113-120, 1952. 29. Koch G: Zur Klinik, Symptomatologie, Pathogenese und Erbpathologie des Klippel-Trénaunay-Weberschen Syndroms . Acta Genet Med Gemel 5( (suppl 1) ):326-370, 1952. 30. Rademacher R: Über einen Fall einer Kombination von Sturge-Weber und Klippel-Trénaunay Syndrom mit konstitutioneller Neurodermitis . Derm Wschr 143:381-384, 1961. 31. Kramer W: Syndromes of Klippel-Trénaunay and Sturge-Weber in the same patient . Psychiat Neurol Neurochir 66:362-370, 1963. 32. Lindgren E: Über corticale Verkalkungen im Gehirn. Nervenarzt 12:138-142, 1939. 33. Schnyder UW, Landolt E, Martz G: Syndrome de Klippel-Trénaunay avec colobome irien atypique . J Genet Hum 5:1-8, 1956. 34. Peters G: Sturge-Webersche Krankheit . Henke-Lubarsch-Rössle Handbuch der spezifische pathologische Anatomie und Histologie . Berlin, Springer-Verlag, 1958, vol 8, p 696.

Journal

Archives of DermatologyAmerican Medical Association

Published: Dec 1, 1970

References