IgG4-positive dacryoadenitis and Küttner submandibular sclerosing inflammatory tumor

Archives of Ophthalmology

Volumn 128, Issue 7, 2010, Pages 942-944

  Jakobiec, Frederick A ^a   Stacy, Rebecca C ^a   Mehta, Manisha ^a   Fay, Aaron ^a  

^a MASSACHUSETTS EYE AND EAR INFIRMARY   (United States)

Author keywords

[No Author keywords available]

Indexed keywords

IMMUNOGLOBULIN G4; PREDNISONE;

AGED; CASE REPORT; CD3+ T LYMPHOCYTE; CHRONIC SCLEROSING SIALADENITIS; COMPUTER ASSISTED TOMOGRAPHY; DIPLOPIA; DRUG DOSE REDUCTION; EXOPHTHALMOS; EYE BIOPSY; EYE PAIN; FEMALE; HUMAN; IN SITU HYBRIDIZATION; KUTTNER TUMOR; LACRIMAL GLAND; LACRIMAL GLAND DISEASE; LACRIMAL GLAND TUMOR; LETTER; PRIORITY JOURNAL; SCLEROSING DACRYOADENITIS; SIALOADENITIS; SUBMANDIBULAR GLAND;

AGED; DACRYOCYSTITIS; FEMALE; GLUCOCORTICOIDS; HUMANS; IMMUNOGLOBULIN G; LACRIMAL APPARATUS; LYMPHOPROLIFERATIVE DISORDERS; PLASMA CELLS; PREDNISONE; SCLEROSIS; SUBMANDIBULAR GLAND DISEASES; TOMOGRAPHY, X-RAY COMPUTED;

EID: 77954994276     PISSN: 00039950     EISSN: 15383601     Source Type: Journal    
DOI: 10.1001/archophthalmol.2010.112     Document Type: Letter

References (12)

1. Kitagawa S, Zen Y, Harada K, et al. Abundant IgG4-positive plasma cell infiltration characterizes chronic sclerosing sialadenitis (Kuttner's tumor). Am J Surg Pathol. 2005;29(6):783-791. (Pubitemid 40734427)
2. Stone JH, Caruso PA, Deshpande V. Case records of the Massachusetts General Hospital: case 24-2009: a 26-year-old woman with painful swelling of the neck. N Engl J Med. 2009;361(5):511-518.
3. Lee LY, Chen TC, Kuo TT. Simultaneous occurrence of IgG4-related chronic sclerosing dacryoadenitis and chronic sclerosing sialadenitis in a patient also with involvement of lymph node and Warthin's tumor [published online December 30, 2008]. Int J Surg Pathol. doi:10.1177/1066896908329584.
4. Kamisawa T, OkamotoA. IgG4-related sclerosing disease. World J Gastroenterol. 2008;14(25):3948-3955.
5. Kamisawa T, Yoshiike M, Egawa N, Nakajima H, Tsuruta K, Okamoto A. Treating patients with autoimmune pancreatitis: results from a long-term follow-up study. Pancreatology. 2005;5(2-3):234-240.
6. Neild GH, Rodriguez-Justo M, Wall C, Connolly JO. Hyper-IgG4 disease: report and characterisation of a new disease. BMC Med. 2006;4:23.
7. Mehta M, Jakobiec F, Fay A. Idiopathic fibroinflammatory disease of the face, eyelids, and periorbital membrane with immunoglobulin G4-positive plasma cells. Arch Pathol Lab Med. 2009;133(8):1251-1255.
8. Cheuk W, Yuen HK, Chan JK. Chronic sclerosing dacryoadenitis: part of the spectrum of IgG4-related sclerosing disease? Am J Surg Pathol. 2007;31(4):643-645.
9. Takahira M, Kawano M, Zen Y, Minato H, Yamada K, Sugiyama K. IgG4-related chronic sclerosing dacryoadenitis. Arch Ophthalmol. 2007;125(11):1575-1578.
10. Sato Y, Ohshima K, Ichimura K, et al. Ocular adnexal IgG4-related disease has uniform clinicopathology. Pathol Int. 2008;58(8):465-470.
11. Cheuk W, Yuen HK, Chan AC, et al. Ocular adnexal lymphoma associated with IgG4+ chronic sclerosing dacryoadenitis: a previously undescribed complication of IgG4-related sclerosing disease. Am J Surg Pathol. 2008;32(8):1159-1167.
12. Ochoa ER, Harris NL, Pilch BZ. Marginal zone B-cell lymphoma of the salivary gland arising in chronic sclerosing sialadenitis (Kuttner tumor). Am J Surg Pathol. 2001;25(12):1546-1550.