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1) Hamano H, Kawa S, Horiuchi A, et al. High serum IgG4 concentrations in patients with sclerosing pancreatitis. N Engl J Med. 2001; 344: 732-8
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2) van der Vliet HJ, Perenboom RM. Multiple pseudotumors in IgG4-associated multifocal systemic fibrosis. Ann Intern Med. 2004; 141: 896-7
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3) Masaki Y, Dong L, Kurose N, et al. Proposal for a new clinical entity, IgG4-positive multiorgan lymphoproliferative syndrome: analysis of 64 cases of IgG4-related disorders. Ann Rheum Dis. 2009; 68: 1310-5
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4) Yamamoto M, Takahashi H, Naishiro Y, et al. Mikuliczʼs disease and systemic IgG4-related plasmacytic syndrome (SIPS). Nihon Rinsho Meneki Gakkai Kaishi. 2008; 31: 1-8. Review
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5) Kamisawa T, Okamoto A. Autoimmune pancreatitis: proposal of IgG4-related sclerosing disease. J Gastroenterol. 2006; 41: 613-25
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6) Neild GH, Rodriguez-Justo M, Wall C, et al. Hyper-IgG4 disease: report and characterisation of a new disease. BMC Med. 2006; 4: 23
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7) Umehara H, Okazaki K, Masaki Y, et al. A novel clinical entity, IgG4-related disease (IgG4RD): general concept and details. Mod Rheumatol. 2011 Sep 1. [Epub ahead of print]
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8) Chari ST, Smyrk TC, Levy MJ, et al. Diagnosis of autoimmune pancreatitis: the Mayo Clinic experience. Clin Gastroenterol Hepatol. 2006; 4: 1010-6
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9) Otsuki M, Chung JB, Okazaki K, et al. Asian diagnostic criteria for autoimmune pancreatitis: consensus of the Japan-Korea Symposium on Autoimmune Pancreatitis. J Gastroenterol. 2008; 43: 403-8. Review
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10) Masaki Y, Umehara H. IgG4-related disease-the diagnostic confusion and how to avoid it. Nihon Rinsho Meneki Gakkai Kaishi. 2009; 32: 478-83. Review. Japanese
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11) Leporati P, Landek-Salgado MA, Lupi I, et al. IgG4-related hypophysitis: a new addition to the hypophysitis spectrum. J Clin Endocrinol Metab. 2011; 96: 1971-80
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12) Wong S, Lam WY, Wong WK, et al. Hypophysitis presented as inflammatory pseudotumor in immunoglobulin G4-related systemic disease. Hum Pathol. 2007; 38: 1720-3
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13) Yamamoto M, Takahashi H, Ohara M, et al. A case of Mikuliczʼs disease (IgG4-related plasma-cytic disease) complicated by autoimmune hypo-physitis. Scand J Rheumatol. 2006; 35: 410-1
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14) Tanabe T, Tsushima K, Yasuo M, et al. IgG4-associated multifocal systemic fibrosis compli-cating sclerosing sialadenitis, hypophysitis, and retroperitoneal fibrosis, but lacking pancreatic involvement. Intern Med. 2006; 45: 1243-7
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15) Ralli S, Lin J, Farrell J. Autoimmune pancreatitis. N Engl J Med. 2007; 356: 1586
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16) Isaka Y, Yoshioka K, Nishio M, et al. A case of IgG4-related multifocal fibrosclerosis complicated by central diabetes insipidus. Endocr J. 2008; 55: 723-8
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17) Tsuboi H, Inokuma S, Setoguchi K, et al. Inflammatory pseudotumors in multiple organs associated with elevated serum IgG4 level: recovery by only a small replacement dose of steroid. Intern Med. 2008; 47: 1139-42
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18) Osawa S, Ogawa Y, Watanabe M, et al. Hypo-physitis presenting with atypical rapid deteriora-tion: with special reference to immunoglobulin G4-related disease--case report--. Neurol Med Chir (Tokyo). 2009; 49: 622-5
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19) Haraguchi A, Era A, Yasui J, et al. Putative IgG4-related pituitary disease with hypopituitarism and/or diabetes insipidus accompanied with elevated serum levels of IgG4. Endocr J. 2010; 57: 719-25
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20) Hori M, Makita N, Andoh T, et al. Long-term clinical course of IgG4-related systemic disease accompanied by hypophysitis. Endocr J. 2010; 57: 485-92
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21) Caturegli P, Lupi I, Landek-Salgado M, et al. Pituitary autoimmunity: 30 years later. Autoimmun Rev. 2008; 7: 631-7. Review
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22) Caturegli P, Newschaffer C, Olivi A, et al. Autoimmune hypophysitis. Endocr Rev. 2005; 26: 599-614
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23) Chan SK, Cheuk W, Chan KT, et al. IgG4-related sclerosing pachymeningitis: a previously unrecognized form of central nervous system involvement in IgG4-related sclerosing disease. Am J Surg Pathol. 2009; 33: 1249-52
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24) Kosakai A, Ito D, Yamada S, et al. A case of definite IgG4-related pachymeningitis. Neurology. 2010; 75: 1390-2
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25) Riku S, Hashizume Y, Yoshida M, et al. Is hypertrophic pachymeningitis a dural lesion of IgG4-related systemic disease? Rinsho Shinkeigaku. 2009; 49: 594-6. Japanese
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26) Lindstrom KM, Cousar JB, Lopes MB. IgG4-related meningeal disease: clinico-pathological features and proposal for diagnostic criteria. Acta Neuropathol. 2010; 120: 765-76. Review
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27) Choi SH, Lee SH, Khang SK, et al. IgG4-related sclerosing pachymeningitis causing spinal cord compression. Neurology. 2010; 75: 1388-90
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28) Kato K, Tamano Y, Namioka A, et al. Hyper-trophic pachymeningitis associated with auto-immune pancreatitis examined for IgG4 related disease: a case report. No Shinkei Geka. 2011; 39: 763-8. Japanese
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29) Takahashi R, Oyamada T, Ozaki H, et al. Three cases of optic neuropathy associated with hyper-trophic pachymeningitis. Nihon Ganka Gakkai Zasshi. 2011; 115: 602-10. Japanese
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30) Kim EH, Kim SH, Cho JM, et al. Immunoglobulin G4-related hypertrophic pachymeningitis involving cerebral parenchyma. J Neurosurg. 2011 Aug 19. [Epub ahead of print]
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31) Kamisawa T, Chen PY, Tu Y, et al. Autoimmune pancreatitis metachronously associated with retroperitoneal fibrosis with IgG4-positive plasma cell infiltration. World J Gastroenterol. 2006; 12: 2955-7
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32) Shrestha B, Sekiguchi H, Colby TV, et al. Distinctive pulmonary histopathology with increased IgG4-positive plasma cells in patients with autoimmune pancreatitis: report of 6 and 12 cases with similar histopathology. Am J Surg Pathol. 2009; 33: 1450-62
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33) Matsushita T, Murai H, Kawajiri M, et al. Character changes from idiopathic cranial pachymeningoencephalitis. J Neurol Sci. 2006; 244: 163-6
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34) Kadoya C, Soejima T, Yamada H, et al. Pachymeningoencephalitis: case report. Neurosurgery. 1993; 33: 131-4
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35) Kupersmith MJ, Martin V, Heller G, et al. Idiopathic hypertrophic pachymeningitis. Neurology. 2004; 62: 686-94
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36) Nishizaki T, Iwamoto F, Uesugi S, et al. Idiopathic cranial pachymeningoencephalitis focally affecting the parietal dura mater and adjacent brain parenchyma: case report. Neurosurgery. 1997; 40: 840-3
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37) Lu YR, Yeh JH, Tsai MD, et al. Focal idiopathic hypertrophic pachymeningoencephalitis. J Formos Med Assoc. 2008; 107: 181-4
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38) Nakazaki H, Tanaka T, Isoshima A, et al. Idiopathic hypertrophic cranial pachymeningitis with perifocal brain edema--case report. Neurol Med Chir (Tokyo). 2000; 40: 239-43
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39) Shimooka N, Utsunomiya R, Kubo S, et al. Pachymeningoencephalitis: case report. [Article in Japanese] No Shinkei Geka. 2005; 33: 595-8
医学中央雑誌刊行会  PubMed 医書jp
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40) Tuncel D, Yücesan C, Erden E, et al. Idiopathic hypertrophic cranial pachymeningitis with perifocal brain edema. Clin Neurol Neurosurg. 2005; 107: 249-52
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