Auszug
Eine Vielzahl angeborener, entzündlicher und verletzungsbedingter Erkrankungen können das wachsende Skelettsystem befallen. Zur Diagnose der orthopädischen Erkrankungen gehören die sorgfältige Anamnese und eine systematische klinische Untersuchung (Buckup 2005). Die Untersuchung muss in den typischen menschlichen Positionen des Stehens, Gehens und Liegens vorgenommen werden. Hierdurch bekommt man einen Eindruck, wie sich der Patient bewegt (⊡ Abb. 12.1) und wie er sich aufrichtet. Einige Erkrankungen wie z. B. Fehlhaltungen der Wirbelsäule, Fußfehlstellungen, Beinachsenfehler und Lähmungen können so schnell aufgedeckt werden.
Access this chapter
Tax calculation will be finalised at checkout
Purchases are for personal use only
Preview
Unable to display preview. Download preview PDF.
Literatur
Abdon P, Bauer M (1989) Incidence of meniscal lesions in children. Increase associated with diagnosis arthroscopy. Acta Orthop Scand 60: 710–711
Aichroth P, Patel D, Zorilla P (2002) The natural history and treatment of rupture of the anterior eruciet ligament in children and adolecents. J Bone Joint Surg Br 84: 38–41
Aglietti P et al. (1995) Arthroscopic meniscectomy for discoid lateral meniscus in children und adolescents: 10-year follow-up. AM J Knee Surg 12: 83–87
Asig M et al. (2003) Discoid lateral menicus: diagnosis and results of artroskopic treatment. Knee Surg Sports Traumatol Arthrosc 11: 99–104
Barker DJ, Hahl AJ (1986) The epidemiology of Perthes disease. Clin Orthop 209: 89–94
Bruns J (1996) Osteochondrosis dissecans. Enke, Stuttgart
Buckup K (2001) Kinderorthopädie. Thieme, Stuttgart
Buckup K (2005) Klinische Tests an Knochen, Gelenken und Muskeln. Thieme, Stuttgart
Campanacci M (1990) Bone and soft tissue tumors. Springer, Wien
Catteral A (1971) The natural history of Perthes disease. J Bone Joint Surg Br 53: 37–53
Coates CJ, Peterson JM, Woods KR et al. (1990) Femoral osteotomy in Perthes’ disease. Results at maturity. J Bone Joint Surg Br 72: 581–585
Debrunner AM (2002) Orthopädie — Orthopädische Chirurgie, 4. Aufl. Huber, Bern
Ekkernkamp A et al. (1990) Die kontinuiertliche Dekompression. Ein neuer Weg in der Behandlung juveniler Knochenzysten. Unfallchirurg 93: 539–543
Fulkerson JP (2002) Diagnosis and treatment of patients with patellofemoral pain. Am J Sports Med 30: 447–456
Grelsamer RP (2000) Patellar malalignement. Current concepts review. J Bone Joint Surg Am 82: 1639–1650
Healy JH, Ghelman B (1986) Osteoid osteoma and osteoblastoma. Clin Orthop 204: 76–85
Hefti F (1997) Heute Knieschmerzen — morgen Sportkrüppel? Schmerzsyndrome am Kniegelenk und Unterschenkel. In: Hefti F (Hrsg) Kinderorthopädie in der Praxis. Springer, Berlin Heidelberg New York Tokio, S 297–305
Hefti F (1999) Foot-pain. Fußschmerzen. Orthopäde 28: 173–179
Hefti F (2006) Kinderorthopädie in der Praxis, 2. Aufl. Springer, Berlin Heidelberg New York Tokio
Hefti F, Jundt G (1994) Welche Tumoren können in der Epiphyse entstehen? Eine Untersuchung aus dem Baseler Knochentumor-Referenzzentrum. Orthopädie Mitteilungen DGOT 24: 153
Hefti F, Jundt G (1995) Langerhans-Zellhistiozytose. Orthopäde 24: 73–78
Hefti F et al. (1999) Osteochondritis dissecans: a multicenter study of the European Pediatric Orthopedic Society. J Pediatr rthop B 8: 231–245
Jerosch J, Mamsch H (1998) Fehlformen und Fehlhaltung kindlicher Füße. Z Orthop 136: 215–220
Kannus P (1988) Long-term results of conservatively treated medial collateral injuries of the knee joint. Clin Orthop 226: 103–112
Köhler A (1913) Das Köhlersche Knochenbild des Os naviculare pedis bei Kindern — Keine Fraktur. Langenbecks Arch Klein Chir 101:560
Köhler A (1920) Eine typische Erkrankung des 2. Metatarsophalangealgelenkes. MMW 45: 1289–1290
Kuwabaras S, Takahashi M (1990) Eosinophilic granuloma of the skull in identical twins case report. Neurol Med Chir (Tokyo) 30: 1043–1046
Laer L (2001) Frakturen und Luxationen im Wachstumsalter, 4. Aufl. Springer, Berlin Heidelberg New York Tokio
Marcove RC (1984) The surgery of tumors of bone and cartilage. Grune & Stratton, Orlando
Meurer AM, Peetz S, Giesa M, Heine J (2002) Der Morbus Scheuermann. Scheuermann’s Disease. Zentralbl Kinderchir 11: 209–213
Nottage W, Matsuura P (1994) Management of complete traumatic anterior cruciate ligament tears in the skelettaly immature patient: Current concepts and review of the literature. Arthroscopy 10: 569–573
Oostvogel HJ, Klasen HJ, Reddingins RE (1988) Fractures of the inter-condylar eminence in children and adolescents. Arch Orthop Trauma Surg 107: 242–247
Ozaki T, Liljenqvist U, Hillmenn A et al. (2002) Osteoid osteome and osteoblastome of the spine: experiences with 22 patients. Clin Orthop 397: 394–402
Papagelopoulos PJ, Galanis EC, Sim FH (1999) Clinicopathologic features, diagnosis, and treatment of osteoblastoma. Orthopedics 22: 244–247
Parsch K, Haesen D (1994) Spontanverlauf des Morbus Perthes. Orthopäde 23: 200–205
Parsch K et al. (1995) Die juvenile Knochenzyste. Stellenwert und Therapieergebnisse der Kortisoninjektion. Orthopäde 24: 65–72
Peterson HA (1994) Deformities and problems of the forearm in children with multiple hereditary osteochondromata. J Pediatr Orthop 14: 92–100
Raber DA (1998) Discoid lateral meniscus in children. Long term follow-up after total meniscectomy. J Bone Joint Surg Am 80: 1579–1586
Robertson W, Kelly BT, Green DW (2003) Osteochondrosis diissecans of the knee in children. Curr Opin Pediatr 15: 38–44
Rosenthal DI et al. (1992) Ablation of osteoid-osteomas with percutaneously placed electrode: A new procedure. Radiology 183: 29–33
Rühmann O, Lazovic D, Wirth CJ et al. (1997) Morbus Perthes — Ergebnisse eines am Containment orientierten Therapiekonzepts. Z Orthopädie Grenzgebiete 135: 232–251
Schai P et al. (1996) Disctrete synchronons multifocal osteoid osteoma of the humerus. Skeletal Radiol 25: 667–670
Stanitski CL (1993) Anterior knee pain syndromes in the adolescent. J Bone Joint Surg Am 75: 1407–1416
Stanitski CL, Harvell JC, Fu F (1993) Observations on acute knee hemarthrosis in children and adolescents. J Pediatr Orthop 13
Venbrocks RT, Albrecht T (1992) Ergebnisse der konservativen und operativen Therapie der Osteochondrosis dissecans des Kniegelenks. Arthroskopie 5: 6–9
Wagenknecht C et al. (1990) Diagnostische Wertigkeit der Skelettszintigrafie im Vergleich zur Röntgenuntersuchung bei der Histiozytose im Kindesalter. Erfahrungsbericht. Kinderärztl Prax 58: 355–362
Windhager R et al. (1995) Die aneurysmatische Knochenzyste. Orthopäde 24: 57–64
Winter RB (1983) Congenital deformities of the spine. Thieme & Stratton, New York
Woods GW, Whelan JM (1990) Discoid meniscus. Clin Sports Med 9: 695–706
Zollinger H (1986) Osteonekrosen am kindlichen Fuß. Orthopäde 15: 220–226
Literatur
De Pellegrin M, Fracassetti D, Ciampi P (1997) Transiente Synovitis des Höftgelenkes. Orthopäde 26: 858–867
Huppertz H-I (1998) Gelenkschmerzen im Kindesalter. Monatsschr Kinderheilkd 146: 5–11
Literatur
Agostoni et al. (2004) Hereditary and acquired angioedema: problems and progress: proceedings of the third C1 esterase inhibitor deficiency workshop and beyond. J Allergy Clin Immunol 114(Suppl): S51–131
Aleman K, Noordzij JG, de Groot R, van Dongen JJ, Hartwig NG (2001) Reviewing Omenn syndrome. Eur J Pediatr 160: 718–725
Amrolia P, Gaspar HB, Hassan A et al. (2000) Nonmyeloablative stem cell transplantation for congenital immunodeficiencies. Blood 96:1239–1246
Ancliff PJ et al. (2001) Mutations in the ELA2 gene encoding neutrophil elastase are present in most patients with sporadic severe congenital neutropenia but only in some patients with the familial form of the disease. Blood 98: 2645–2650
Antoine C et al., European group for Blood and Marrow transplantation (2003) Long term survival and hematopoetic stem cell transplantation for immunodeficiencies. A survey of European experiences 1968–1999. Lancet 361:553–560
Barbosa MD et al. (1996) Identification of the homologous beige and Chediak-Higashi syndrome genes. Nature 382: 262–265
Benkerrou M, Le Deist F, de Villartay JP et al. (1997) Correction of Fas (CD95) deficiency by haploidentical bone marrow transplantation. Eur J Immunol 27: 2043–2047
Bruton OC (1952) Agammaglobulinemia. Pediatrics 9: 722–728
Buckley RH (2002) Immunoglobulin G Subclass Deficiency: Fact or Fancy. Curr Allergy Asthma Rep 2: 356–360
Buckley RH (2004) Molecular defects in human severe combined immunodeficiency and approaches to immune reconstitution. Annu Rev Immunol 22: 625–655
Bunting M, Harris E, McIntyre T et al. (2002) Leukocyte adhesion deficiency syndromes: adhesion and tethering defects involving beta 2 integrins and selectin ligands. Curr Op Hematol 9: 30–35
Burrows PD, Cooper MD (1997) IgA deficiency. Adv Immunol. 65: 245–276
Canale VC, Smith CH (1997) Chronic lymphadenopathy simulating malignant lymphoma. J Pediatr 70: 891–899
Chun HJ, Zheng L, Ahmad M et al. (1997) Pleiotropic defects in lymphocyte activation caused by caspase-8 mutations lead to human immunodeficiency. Nature 419: 395–399
Conley M (1999) Autosomal recessive agammaglobulinemia. In: Ochs, H. D.; Smith, C. I. E.; Puck, JM (eds) Primary Immunodeficiency Diseases: A Molecular and Genetic Approach. Oxford University Press, pp 285–291
Conley ME, Mathias D, Treadaway J, Minegishi Y, Rohrer J (1998) Mutations in Btk in patients with presumed X-linked agammaglobulinemia. Am J Hum Genet 62: 1034–1043
Conley ME, Howard V (2002) Clinical findings leading to the diagnosis of X-linked agammaglobulinemia. J Pediatr 141: 566–571
Courtois G, Smahi A, Reichenbach J et al. (2003) A hypermorphic IkappaBalpha mutation is associated with autosomal dominant anhidrotic ectodermal dysplasia and T cell immunodeficiency. J Clin Invest 112: 1108–15
Cunningham-Rundles C (2001) Common variable immunodeficiency. Curr Allergy Asthma Rep 1: 421–429
Dadi HK, Simon AJ, Roifman CM (2003) Effect of CD3delta deficiency on maturation of alpha/beta and gamma/delta T-cell lineages in severe combined immunodeficiency. New England J Med 349: 1821–1828
Dale DC (1998) Immune and idiopathic neutropenia. Curr Opin Hematol 5: 33–36
Dianzani U, Bragardo M, DiFranco D, Alliaudi C, Scagni P, Buonfiglio D, Redoglia V, Bonissoni S, Correra A, Dianzani I, Ramenghi U (1997) Deficiency of the Fas apoptosis pathway without Fas gene mutations in pediatric patients with autoimmunity/lymphoproliferation. Blood 89: 2871–2879
Doffinger R, Smahi A, Bessia C et al. (2001) X-linked anhidrotic ectodermal dysplasia with immunodeficiency is caused by impaired NF-kappaB signaling. Nat Genet 27: 277–285
Dror Y, Freedman HM (2002) Shwachman-Diamond syndrome. Brit J Haematol 118: 701–713
Dupuis-Girod S, Medioni J, Haddad E et al. (2003) Autoimmunity in Wiskott-Aldrich syndrome: risk factors, clinical features, and outcome in a single-center cohort of 55 patients. Pediatrics 111, e622–627111:e622–627
Eijkhout HW, van der Meer JW, Kallenberg CG, Weening RS, van Dissel JT, Sanders LA, Strengers PF, Nienhuis H, Schellekens PT (2001) The effect of two different dosages of intravenous immunoglobulin on the incidence of recurrent infections in patients with primary hypogammaglobulinemia. A randomized, double-blind, multicenter crossover trial. Ann Intern Med 135: 165–174
Feldmann J, Callebaut I, Raboso G et al. (2003) Munc13-4 is essential for cytolytic granule fusion and is mutated in a form of familial hemophagocytic lymphohistiocytosis (FHL3). Cell 115: 461–473
Filipovich AH, Stone JV, Tomany SC et al. (2001) Impact of donor type on outcome of bone marrow transplantation for Wiskott-Aldrich syndrome: collaborative study of the International Bone Marrow Transplant Registry and the National Marrow Donor Program. Blood 97: 1598–1603
Gallin JI, Alling DW, Malech HL, Wesley R, Koziol D, Marciano B, Eisenstein EM, Turner ML, DeCarlo ES, Starling JM, Holland SM (2003) Itraconazole to prevent fungal infections in chronic granulomatous disease. N Engl J Med 348: 2416–2422
Gardulf A, Andersen V, Björkander J, Ericson D, Fröland SS, Gustafson R, Hammarström L, Jacobsen MB, Jonsson E, Möller G, Nyström T, Söeberg B, Smith CIE (1995) Subcutaneous immunoglobulin replacement in patients with primary antibody deficiencies: safety and costs. The Lancet 345: 365–369
Gaspar HB, Lester T, Levinsky RJ, Kinnon C (1998) Bruton’s tyrosine kinase expression and activity in X-linked agammaglobulinaemia (XLA): the use of protein analysis as a diagnostic indicator of XLA. Clin Exp Immunol 111: 334–338
Gennery AR, Barge D, O’Sullivan JJ et al. (2002) Antibody deficiency and autoimmunity in 22q11.2 deletion syndrome. Arch Dis Child 86: 422–425
Giliani S, Mori L, de Saint Basile G et al. (2005) Interleukin-7 receptor alpha (IL-7Ralpha) deficiency: cellular and molecular bases. Analysis of clinical, immunological, and molecular features in 16 novel patients. Immunological Reviews 203: 110–126
Goldblatt D (2002) Current treatment options for CGD. Exp Opin Pharmacother 3: 857–863
Grimbacher B, Hutloff A, Schlesier M et al. (2003) Homozygous loss of ICOS is associated with adult-onset common variable immunodeficiency. Nature Immunol 4: 261–268
Gulino AV, Notarangelo LD (2003) Hyper IgM syndromes. Curr Opin Rheumatol 15: 422–429
Haas JP, Grunke M, Frank C et al. (1997) Increased spontaneous in vitro apoptosis in double negative T cells of humans with a fas/apo-1 mutation. Cell Death Differ 5: 751–757
Habermehl P, Zepp F (2005) Störungen der zellulären Immunfunktion. In: Wahn U, Seger R, Wahn V, Holländer GA (Hrsg) Pädiatrische Allergologie und Immunologie, 4. Aufl. Urban & Fischer, München
Hammarström L, Vořechovský I, Webster D (2000) Selective IgA deficiency (SIgAD) and common variable immundeficiency (CVID) Clin Exp Immunol 120: 225–231
Henter JI, Samuelsson-Horne A, Arico M et al. (2002) Treatment of hemophagocytic lymphohistiocytosis with HLH-94 immunochemotherapy and bone marrow transplantation. Blood 100: 2367–2373
Hernandez PA, Gorlin RJ, Lukens JN, Taniuchi S, Bohinjec J, Francois F, Klotman ME, Diaz GA (2003) Mutations in the chemokine receptor gene CXCR4 are associated with WHIM syndrome, a combined immunodeficiency disease. Nat Genet 34: 70–74
Horwitz M et al. (1999) Mutations in ELA2, encoding neutrophil elastase, define a 21-day biological clock in cyclic hematopoiesis. Nat Genet 23: 433–436
Hubert A, Baumann U, Borte M, Habermehl P, Schulze I, Schuster V, Wolf H, Grimbacher B (2004) Humorale Immundefizienz I: Antikörpermangelsyndrome ohne bekannten genetischen Defekt. Allergologie 27: 296–310
Imashuku S et al. (1999) Effective control of Epstein-Barr virus-related hemophagocytic lymphohistiocytosis with immunochemotherapy. Histiocyte society. Blood 93: 1869–1874
International CGD Cooperative Study Group (1991) A controlled trial of interferon gamma to prevent infection in chronic granulomatous disease. N Engl J Med 324: 509–516
Kamani NR, Infante AJ (2000) Chronic granulomatous disease and other disorders of neutrophil function. Clin Rev Allergy Immunol 19: 141–156
Kilic SS, Tezcan I, Sanal Ö, Metin A, Ersoy F (2000) Transient hypogammaglobulinemia of infancy: Clinical and immunologic features of 40 new cases. Pediatrics Int 42: 647–650
Lindvall JM, Blomberg KE, Valiaho J, Vargas L, Heinonen JE, Berglof A, Mohamed AJ, Nore BF, Vihinen M, Smith CIE (2005) Bruton’s tyrosine kinase: cell biology, sequence conservation, mutation spectrum, siRNA modifications, and expression profiling. Immunol Rev 203: 200–215
Litzman J, Jones A, Hann I, Chapel H, Strobel S, Morgan G (1996) Intravenous immunoglobulin, splenectomy, and antibiotic prophylaxis in Wiskott-Aldrich syndrome. Arch Dis Child 75: 436–439
Macchi P et al. (1995) Mutations of Jak-3 gene in patients with autosomal severe combined immune deficiency (SCID). Nature 377: 65–68
Mannhardt-Laakmann W, Habermehl P, Knuf M, Schaaf F, Zepp F, Ehl S (2004) Impfungen bei Immundefizienz. Kinderärztliche Praxis 4: 214–229
Markert ML (1991) Purine nucleoside phosphorylase deficiency. Immunodefic Rev 3: 45–81
Markert ML et al. (2003) Thymus transplantation in complete DiGeorge syndrome: immunologic and safety evaluations in 12 patients. Blood 102: 1121–1130
Martin DA, Zheng L, Siegel RM et al. (1999) Defective CD95/APO-1/Fas signal complex formation in the human autoimmune lymphoproliferative syndrome, type Ia. Proc Natl Acad Sci USA 96: 4552–4557
McKinney RE Jr, Katz SL, Wilfert CM (1987) Chronic enteroviral meningoencephalitis in agammaglobulinemic patients. Rev Infect Dis 9: 334–356
Menasche G, Pastural E, Feldmann J et al. (2000) Mutations in RAB27A cause Griscelli syndrome associated with hemophagocytic syndrome. Nat Genet 25: 173–176
Muller SM, Ege M, Pottharst A, Schulz AS, Schwarz K, Friedrich W (2001) Transplacentally acquired maternal T lymphocytes in severe combined immunodeficiency: a study of 121 patients. Blood 98: 1847–1851
Niehues T, Weiß M, Wahn V (2005) http://www.immundefekte.de/klass 2005
Noguchi M et al. (1993) Interleukin-2 receptor gamma chain mutation results in X-linked severe combined immunodeficiency in humans. Cell 73: 147–157
Notarangelo L, Casanova JL, Fischer A, Puck J, Rosen F, Seger R, Geha R (2004) International Union of Immunological Societies Primary Immunodeficiency diseases classification committee. Primary immunodeficiency diseases: an update. J Allergy Clin Immunol 114: 677–687
O’Driscoll M, Gennery AR, Seidel J, Concannon P, Jeggo PA (2004) An overview of three new disorders associated with genetic instability: LIG4 syndrome, RS-SCID and ATR-Seckel syndrome. DNA Repair 3: 1227–1235
Pan Q, Hammarstrom L (2000) Molecular basis of IgG subclass deficiency. Immunol Rev 178: 99–110
Picard C et al. (2003) Pyogenic bacterial infections in humans with IRAK-4 deficiency. Science 299: 2076–2079
Perez EF et al. (2003) Safety of live viral vaccine in patients with chromosome 22q11.2 deletion dyndrome. Pediatrics 112: e325
Pignata C (2002) A lesson for unraveling complex aspects of novel immunodeficiencies from the human equivalent of the nude/SCID phenotype. J Hematother Stem Cell Res 11: 409–414
Puck JM, Straus SE, LeDeist F, Rieux-Laucat F, Fisher A (2000) Inherited disorders with autoimmunity and defective lymphocyte regulation. In: Ochs HD, Smith CIE, Puck J (eds) Primary immunodeficiency diseases, a molecular and genetic approach. Oxford University Press, pp 339–352
Rieux-Laucat F, Le Deist F, Fischer A (2003) Autoimmune lymphoproliferative syndromes: genetic defects of apoptosis pathways. Cell Death Differ 10: 124–133
Ryan AK et al. (1997) Spectrum of clinical features associated with interstitial chromosome 22q11 deletions. a European collaborative study. J Med Genet 34: 798–804
Ryser O, Morell A, Hitzig W (1988) Primary immunodeficiencies in Switzerland: First report of the national registry in adults and children. J Clin Immunol 8: 479–485
Salzer U, Maul-Pavicic A, Cunningham-Rundles C, Urschel S, Belohradsky BH, Litzmann J, Holm A, Franco JL, Plebani A, Hammarstrom L, Skrabl A, Schwinger W, Grimbacher B (2004) ICOS-deficiency in patients with common variable immunodeficiency. Clin Immunol 113: 234–240
Savitzky K, Sfez S, Tagle DA, Ziv Y, Sartiel A, Collins FS, Shiloh Y, Rothman G (1995) The complete sequence of the coding region of the ATM gen reveals similarity to cell cycle regulators in different species. Hum Mol Genet 4: 2025–2032
Seger RA, Gungor T, Belohradsky BH et al. (2002) Treatment of chronic granulomatous disease with myeloablative conditioning and an unmodified hemopoietic allograft: a survey of the European experience, 1985–2000. Blood 100: 4344–4350
Schneider EM, Lorenz I, Muller-Rosenberger M et al. (2002) Hemophagocytic lymphohistiocytosis is associated with deficiencies of cellular cytolysis but normal expression of transcripts relevant to killer cell apoptosis. Blood 100: 2891–2898
Spickett GP (2001) Current perspectives on common variable immunodeficiency (CVID) Clin Exp Allergy 31: 536–542
Stengaard-Pedersen K, Thiel S, Gadjeva M, Moller-Kristensen M, Sorensen R, Jensen LT, Sjoholm AG, Fugger L, Jensenius JC (2003) Inherited deficiency of mannan-binding lectin-associated serine protease 2. N Engl J Med 349: 554–560
Stepp SE et al. (1999) Perforin gene defects in familial hemophagocytic lymphohistiocytosis. Science 286: 1957–1959
Straus SE, Jaffe ES, Puck JM et al. (2001) The development of lymphomas in families with autoimmune lymphoproliferative syndrome with germline Fas mutations and defective lymphocyte apoptosis. Blood 98: 194–200
Wahn V, Späth PJ (2005) Hereditäre Komplementdefekte. In: Wahn U, Seger R, Wahn V, Holländer GA (Hrsg) Pädiatrische Allergologie und Immunologie, 4. Aufl. Urban & Fischer, München
Wang J, Zheng L, Lobito A et al.(1999) Inherited human Caspase 10 mutations underlie defective lymphocyte and dendritic cell apoptosis in autoimmune lymphoproliferative syndrome type II. Cell 98: 47–58
Weemaes CMR, Hustinex TWJ, Scheres JMJC, van Munster PJJ, Bakkeren JAJM, Maalman RDFM (1981) New chromosome instability disorder: The Nijmegen breakage syndrome. Acta Paediatr Scan 70: 557–562
Welte K, Boxer LA (1997) Severe chronic neutropenia: pathophysiology and therapy. Semin Hematol 34: 267–278
Wen L, Atkinson JP, Giclas PC (2004) Clinical and laboratory evaluation of complement deficiency. J Allergy Clin Immunol 113: 585–593
Wurzner R, Orren A, Lachmann PJ (1992) Inherited deficiencies of the terminal components of human complement. Immunodefic Rev 3: 123–147
Literatur
Chung S, Frush DP, Prose NS et al. (1999) Subcutaneous granuloma annulare: MR imaging features in six children an literatur review. Radiology 210: 845–849
Felner EI, Steinberg JB, Weinberg AG (1997) Subcutaneous granuloma annulare: a review of 47 cases. Pediatrics 100: 965–967
Grogg KL, Nascimento AG (2001) Subcutaneous granuloma annulare in childhood: clinicopathologic features in 34 cases. Pediatrics 107:E42
Literatur
Evans AM, Scutter SD (2004) Prevalence of »growing pains« in young children. J Pediatrics 145: 255–258
Hashkes PJ, Friedland O, Jaber L et al. (2004) Decreased pain threshold in children with growing pains. J Rheumatol 31: 610–613
Halliwell P, Monsell F (2001) Growing pains: a diagnosis of exclusion. Practioner 245: 620–623
Literatur
Darville T, Jacobs RF (2004) Management of acute hematogenous osteomyelitis in children. Pediatr Infect Dis J 23: 255–257
Janner D (2005) Osteomyelitis and septic arthritis. In: A clinical guide to pediatric infectious disease, Lippincott Williams & Wilkins, Philadelphia, pp 15–25
Roos R, Belohradsky BH, Dietz HG et al. (2003) Akute haematogene Osteomyelitis, bakterielle Arthritis, Spondylodiszitis. In: Scholz H et al. (Hrsg) Handbuch der Deutschen Gesellschaftfür pädiatrische Infektiologie. Infektionen bei Kindern und Jugendlichen, 4. Aufl. Futuramed, München, S 906–913
Rüggeberg J (2005) Osteomyelitis und Bakterielle Arthritis. In: Wahn V, Dannecker G, Horneff G, Huppertz H-I, Schroten H (Hrsg) Fieber im Kindesalter — Systematik und Differenzialdiagnosen. Hans Marseille, München, S 51–54
Unkila-Kallio MJT, Eskola J, Peltola H (1994) Serum C-reactive protein, erythrocyte sedimentation rate, and white blood cell count in acute hematogenous osteomyelitis of children. Pediatrics 93: 53–62
Literatur
Appell RG, Oppermann HC, Becker W, Kratzat R, Brandeis WE, Willich E (1983) Condensing osteitis of the clavicle in childhood: a rare sclerotic bone lesion. Review of literature and report of seven patients. Pediatr Radiol 13: 3061–3066
Bjorksten B, Gustavson KH, Eriksson B, Lindholm A, Nordstrom S (1978) Chronic recurrent multifocal osteomyelitis and pustulosis palmoplantaris. J Pediatr 93: 227–231
Carr AJ, Cole WG, Roberton DM, Chow CW (1993) Chronic multifocal osteomyelitis. J Bone Joint Surg Br 75: 582–591
Chamot AM, Benhamou CL, Kahn MF, Beraneck L, Kaplan G, Prost A (1987) Acne-pustulosis-hyperostosis-osteitis syndrome. Results of a national survey. 85 cases. Rev Rhum Mal Osteoartic 54: 187–196
Giedion A, Holthusen W, Masel LF, Vischer D (1972) Subacute and chronic »symmetrical« osteomyelitis. Ann Radiol (Paris) 15: 329–342
Girschick HJ, Huppertz HI, Harmsen D, Krauspe R, Muller-Hermelink HK, Papadopoulos T (1999) Chronic recurrent multifocal osteomyelitis in children: diagnostic value of histopathology and microbial testing. Hum Pathol 30: 59–65
Girschick HJ, Krauspe R, Tschammler A, Huppertz HI (1998) Chronic recurrent osteomyelitis with clavicular involvement in children: diagnostic value of different imaging techniques and therapy with non-steroidal anti-inflammatory drugs. Eur J Pediatr 157: 28–33
Girschick HJ, Raab P, Surbaum S et al. (2005) Chronic non-bacterial osteomyelitis in children. Ann Rheum Dis 64: 279–285
Jurik AG, Moller BN (1987) Chronic sclerosing osteomyelitis of the clavicle. A manifestation of chronic recurrent multifocal osteomyelitis. Arch Orthop Trauma Surg 106: 144–151
Kahn MF, Chamot AM (1992) SAPHO syndrome. Rheum Dis Clin North Am 18: 225–246
Kotilainen P, Merilahti-Palo R, Lehtonen OP et al. (1996) Propionibacterium acnes isolated from sternal osteitis in a patient with SAPHO syndrome. J Rheumatol 23: 1302–1304
Schilling F, Wagner AD (2000) Azithromycin: an anti-inflammatory effect in chronic recurrent multifocal osteomyelitis? A preliminary report. Z Rheumatol 59: 352–353
Vittecoq O, Said LA, Michot C et al. (2000) Evolution of chronic recurrent multifocal osteitis toward spondylarthropathy over the long term. Arthritis Rheum 43: 109–119
Wagner AD, Andresen J, Jendro MC, Hulsemann JL, Zeidler H (2002) Sustained response to tumor necrosis factor alpha-blocking agents in two patients with SAPHO syndrome. Arthritis Rheum 46: 1965–1968
Waldvogel K, Regnery RL, Anderson BE, Caduff R, Caduff J, Nadal D (1994) Disseminated cat-scratch disease: detection of Rochalimaea henselae in affected tissue. Eur J Pediatr 153: 23–27
Yu L, Kasser JR, O’Rourke E, Kozakewich H (1989) Chronic recurrent multifocal osteomyelitis. Association with vertebra plana. J Bone Joint Surg Am 71: 105–112
Literatur
Arndt CA, Crist WM (1999) Common musculoskeletal tumors of childhood and adolescence. N Engl J Med 341: 342–352
Barbosa CM, Nakamura C, Terreri MT, Lee ML, Petrilli AS, Hilário MO (2002) Musculoskeletal manifestations as the onset of acute leukemias in childhood. J Pediatr (Rio J) 78: 481–484
Bielack S, Kempf-Bielack B, Delling G et al. (2002) Prognostic factors in high-grade osteosarcoma of the extremities or trunk. An analysis of 1702 patients treated on neoadjuvant Cooperative Osteosarcoma Study Group protocols. J Clin Oncol 20: 776–790
Bielack S, Machatschek JN, Flege S, Jürgens H (2004) Delaying surgery with chemotherapy for osteosarcoma of the extremities. Expert Opin Pharmacother 5: 1243–56
Cabral DA, Tucker LB (1999) Malignancies in children who initially present with rheumatic complaints. J Pediatr 134: 53–57
Costello PB, Brecher ML, Starr JI, Freeman AI, Green FA (1983) A prospective analysis of the frequency, course, and possible prognostic significance of the joint manifestations of childhood leukemia. J Rheumatol 10: 753–757
Gallagher DJ, Phillips DJ, Heinrich SD (1996) Orthopedic manifestations of acute pediatric leukemia. Orthop Clin North Am 27: 635–644
Gonçalves M, Terreri MTRA, Barbosa CMPL, Len CA, Lee L, Hilário MOE (2005) Diagnosis of malignancies in children with musculoskeletal complaints. Sao Paulo Med J 123: 2005
Murray MJ, Tang T, Ryder C, Mabin D, Nicholson JC (2004) Childhood leukaemia masquerading as juvenile idiopathic arthritis. BMJ 329: 959–961
Ostrov BE, Goldsmith DP, Athreya BH (1993) Differentiation of systemic juvenile rheumatoid arthritis from acute leukaemia near the onset of disease. J Pediatr 122: 595–598
Parker BR, Marglin S, Castellino RA (1980) Skeletal manifestations of Leukemia, Hodgkin disease and non-Hodgkin lymphoma. Semin Roentgenol 15: 302–315
Paulussen M, Fröhlich B, Jügens H (2001) Ewing Tumour. Incidence, Prognosis and Treatment Options. Pediatr Drugs 3: 899–913
Pui CH, Schrappe M, Ribeiro RC, Niemeyer CM (2004) Childhood and Adolescent Lymphoid and Myeloid Leukemia. Hematology (Am Soc Hematol Educ Program): 118–145
Révész T, Kardos G, Kajtar P, Schuler D (1985) The adverse effect of prolonged prednisolone pretreatment in children with acute lymphoblastic leukemia. Cancer 55: 1637–1640
Schuck A, Ahrens S, Paulussen M et al. (2003) Local therapy in localized Ewing tumors: results of 1058 patients treated in the CESS 81, CESS 86, and EICESS 92 trials. Int J Radiat Oncol Biol Phys 55: 168–177
Shalaby-Rana E, Majd M (2001) (99m)Tc-MDP scintigraphic findings in children with leukemia: value of early and delayed whole-body imaging. J Nucl Med 42: 878–883
Takagi S, Tanaka O (1996) The role of magnetic resonance imaging in the diagnosis and monitoring of myelodysplastic syndromes or leukemia. Leuk Lymphoma 23: 443–450
Tardivon AA, Vanel D, Munck JN, Bosq J (1997) Magnetic resonance imaging of the bone marrow in lymphomas and leukemias. Leuk Lymphoma 25: 55–68
Virchow R (1845) Weisses Blut. Frorieps Notizen 36: 151–156
Whitlock JA, Gaynon PS (1999) Acute lymphoblastic leukemia. In: Lee GR, Forester J, Lukens J, Paraskevas S, Gree GP, Rodgers GM (eds) Wintrobe’s clinical hematology, 10th edn. Williams & Willkins, Baltimore, pp 2241–2271
Literatur
Burnett MW, Bass JW, Cook BA (1998) Etiology of osteomyelitis complicating sickle cell disease. Pediatrics 101: 296–297
Dickerhoff R, von Ruecker A (2005) Leitfaden für die Betreuung von Sichelzellpatienten. Internet-Neufassung 11/05 der Sichelzellstudie Deutschland
Hilgartner M (2002) Current treatment of hemophilic arthropathy. Curr Op in Pediatr 14: 46–49
Kern M, Blanchette V, Stain A, Einarson T, Feldman B (2004) Clinical cost implications of target joints in canadian boys with severe hemophilia A. J Ped 145: 628–634
Roosendaal G, Lafeber F (2003) Blood-induced joint damage in hemophilia. Semin Thromb Hemost 29: 37–42
Schneppenheim R, Bergmann F (2005) Thrombozyten und Gerinnung. In: Lentze, Schaub, Schulte, Spranger (Hrsg) Pädiatrie, 2. Aufl. Springer, Berlin Heidelberg New York Tokio
Smith JA (1996) Bone disorders in sickle cell disease. Hematol Oncol Clin North Am 10: 1345–1356
Author information
Authors and Affiliations
Editor information
Editors and Affiliations
Rights and permissions
Copyright information
© 2007 Springer Medizin Verlag Heidelberg
About this chapter
Cite this chapter
Buckup, K. et al. (2007). Nichtrheumatische Ursachen von Arthralgien und Arthritiden. In: Wagner, N., Dannecker, G. (eds) Pädiatrische Rheumatologie. Springer, Berlin, Heidelberg. https://doi.org/10.1007/978-3-540-32815-5_12
Download citation
DOI: https://doi.org/10.1007/978-3-540-32815-5_12
Publisher Name: Springer, Berlin, Heidelberg
Print ISBN: 978-3-540-32814-8
Online ISBN: 978-3-540-32815-5
eBook Packages: Medicine (German Language)