Gender differences in COPD : are women more susceptible to smoking effects than men ?


lesions (figure 1). Pancreas biopsies revealed chronic pancreatitis. Accessory salivary gland and coeliac adenopathy biopsies showed noncaseating giant-cell epithelioid granuloma. The tuberculin purified protein derivative test and the Quantiferon assay were both negative. Laboratory analysis revealed a polyclonal hypergammaglobulinemia with IgG level at 35 g/l; serum IgG4 level was increased at 6.8 g/l (normal<0.8 g/l), white blood cell count revealed a lymphopenia (1000 mm/l) and ACE was within the normal range. Because of the histological picture of nontuberculous granulomas, and mediastinal lymph nodes with pulmonary involvement on chest CT, sarcoidosis associated with an IgG4+ MOLPS was diagnosed. Corticosteroids (1 mg/kg/day) led to a dramatic improvement in the general and digestive manifestations within a 1-year follow-up. AIP is a form of chronic pancreatitis characterised by a high serum IgG4 concentration and abundant IgG4-bearing plasma cell infiltration in the pancreatic lesion. This entity has been reported to be associated with a variety of extrapancreatic lesions. It is generally accepted that this form of pancreatitis is a part of a multi-systemic clinical syndrome, and this disease was redefined as ‘IgG4-positive multi-organ lymphoproliferative syndrome’. Recently, Tsushima et al compared the clinicopathological features of pulmonary lesions in 19 patients with AIP and 8 patients with sarcoidosis; 17 of the 19 patients with AIP showed bilateral hilar lymphadenopathy, while 8 showed pulmonary nodules. IgG4-positive plasma cells were identified in the pulmonary lesions of patients with AIP. Our patient presented an authentic chronic pancreatitis with a significant increase in serum IgG4 level. She fulfilled the revised diagnostic criteria for AIP. Because of the presence of pulmonary lesions and hilar lymphadenopathies, salivary gland and coeliac adenopathies were biopsied, and they both revealed non-caseating epithelioid cell granulomas. Although sarcoidosis is uncommon in the elderly, the presence of disseminated granulomatous lesions led us to suspect sarcoidosis. However, it is difficult to determine whether our 80-year-old patient has an IgG4related disease with systemic granulomatous lesions or an association of AIP with true sarcoidosis. To our knowledge, such an association of AIP with granulomatous lesions mimicking sarcoidosis has never been reported previously in the literature, and this enlarges the spectrum of IgG4-related disease.


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