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A case of hypertrophic cranial pachymeningitis associated with invasive Aspergillus mastoiditis.

Okada M1, Hato N2, Okada Y3, Sato E2, Yamada H2, Hakuba N2, Gyo K4.
Auris, nasus, larynx.Auris Nasus Larynx.2015 Dec;42(6):488-91. doi: 10.1016/j.anl.2015.04.009. Epub 2015 May 21.
We report a rare case of hypertrophic cranial pachymeningitis (HCP) associated with invasive Aspergillus mastoiditis. A 63-year-old man with diabetes mellitus underwent mastoidectomy because of chronic discharge from his left ear. The mastoidectomy was unsuccessful in resolving purulent otorrhea; mo
PMID 26003880

George MM1, Goswamy J1, Solanki K2, Bhalla R3.
Annals of medicine and surgery (2012).Ann Med Surg (Lond).2015 Mar 30;4(2):103-6. doi: 10.1016/j.amsu.2015.03.005. eCollection 2015.
Inflammatory skull base masses are enigmatic and often behaviourally unpredictable. We present a case of idiopathic hypertrophic pachymeningitis (IHP) forming a central skull base mass to illustrate the process required when one investigates such skull base lesions. This is the first description of
PMID 25905016

Zhu R1, He Z, Ren Y.
European spine journal : official publication of the European Spine Society, the European Spinal Deformity Society, and the European Section of the Cervical Spine Research Society.Eur Spine J.2015 May;24 Suppl 4:S633-5. doi: 10.1007/s00586-015-3956-4. Epub 2015 Apr 18.
PURPOSE: Hypertrophic craniocervical pachymeningitis (HCP) is a rare disease causing chronic inflammatory hypertrophy of the cranial and spinal dura mater. To increase awareness of this condition, we report the details of a case here.METHODS: We reviewed the case of a 78-year-old man presenting with
PMID 25893340

坂井利行,近藤昌秀,由井進太郎,冨本秀和
臨床神経学 54(8), 664-667, 2014
症例は32歳の女性である．頭痛，視力低下で発症し，尿崩症，球後視神経炎，四肢腱反射亢進と軽度筋力低下を呈し，血清IgG4上昇，髄液細胞数軽度増多と蛋白増加をみとめ，中枢性IgG4関連疾患と診断した．頭部と脊髄造影MRIにて下垂体炎，および頭蓋，頸椎，腰椎と仙椎レベルの肥厚性硬膜炎を，胸部CTで左肺小結節をみとめた．硬膜生検ではリンパ球系細胞浸潤をみとめたがIgG4免疫染色陽性形質細胞はみられなかっ …
NAID 130004679011