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. 2017 Mar 31;8(1):e5. doi: 10.5037/jomr.2017.8105

Table 2.

Reported cases of MALT lymphoma of the minor salivary glands in Sjögren’s syndrome patients

Author Year No. of cases Age Sex Oral location Other locations Risk factors Treatment Follow-up
Speight et al. [23] 1994 4 NR NR Lipa Stomach NR NR NR

NR NR Lipa Palate NR NR NR

NR NR Lipa Cervical lymph nodes NR NR NR

NR NR Lipa Cervical lymph nodes NR NR NR

Van Mello et al. [24] 2005 3 53 F Lipb Possibly chest area Non-blanching purpuric lesions on the lower limbs, C4 low NR NR

51 F Lipb NR Intermittent swollen parotids, raised levels of total protein,
IgG, IgA, IgM, while C4 levels and white blood cell count were decreased
NR NR

55 Lipa NR Intermittent swelling of the parotid gland Leukeran (4 mg daily)
and prednisone 20 mg/day
NR

Pijpe et al. [25] 2005 1 42 F Hard palateb Right Parotid 10 years
earlier neck lymph nodes
Increased IgG Weekly, course of 4 infusions of rituximab NS, no recurrence

Sakuma et al. [26] 2006 1 70 F Hard palatea - - Self regression 38 months, no recurrence

Keszler et al. [27] 2012 1 60 F Lipa - - Watch and wait Evaluation performed every 6 months during
the first year and then, once a year, no recurrence

Shwetha et al. [28] 2014 1 62 F Upper and
lower lipb
- - Watch and wait NS, no recurrence

Present case 2017 1 64 F Hard
palatea
Stomach; spleen; bone marrow CD4 + T lymphocytopenia, neutropenia, high serum β2 microglobulin, low serum IgM levels Refused treatment for 1 year
(Rituximab + Fludarabine)
2 years, no recurrence

aMALT lymphoma diagnosed after Sjögren’s syndrome initial diagnosis.

bMALT lymphoma diagnosed simultaneously with Sjögren’s syndrome.

NR = not reported; F = female; NS = not specified.