Idiopathic Tumefactive Chronic Pancreatitis: Clinical Profile, Histology, and Natural History After Resection

被引:102
作者
Yadav, Dhiraj [1 ]
Notahara, Kenji [2 ]
Smyrk, Thomas C. [2 ]
Clain, Jonathan E. [1 ]
Pearson, Randall K. [1 ]
Farnell, Michael B. [3 ]
Chari, Suresh T. [1 ]
机构
[1] Mayo Clin, Div Gastroenterol & Hepatol, Rochester, MN 55905 USA
[2] Mayo Clin, Div Anat Pathol, Rochester, MN 55905 USA
[3] Mayo Clin, Div Gastroenterol & Gen Surg, Rochester, MN 55905 USA
关键词
D O I
10.1053/cgh.2003.50016
中图分类号
R57 [消化系及腹部疾病];
学科分类号
摘要
Background & Aims: Little is known about subjects with idiopathic tumefactive chronic pancreatitis (TCP), that is, chronic pancreatitis whose clinical presentation, usually with a mass or obstructive jaundice, suggests cancer. Methods: We independently reviewed clinical data and histology of 45 TCP (27 idiopathic, 18 alcohol induced) resected at Mayo Clinic (January 1985-March 2001). Follow-up data were obtained from medical records and mailed questionnaires. Results: Compared with alcoholic subjects, idiopathic TCP patients were older (58 +/- 2 vs. 48 +/- 3 yr, P < 0.001), had shorter symptom duration (median 3 vs. 24 wk, P < 0.001), were more likely to have no or mild abdominal pain (70% vs. 17%, P = 0.001), and were more often jaundiced (67% vs. 33%, P = 0.02). Three distinct histologic patterns were identified in TCP. Typical CP (n = 19) showed lobular atrophy, fat necrosis, and ductal changes (dilatation, protein plugs, and stones). Lymphoplasmacytic sclerosing pancreatitis (LPSP) (n = 14) was characterized by periductal lymphoplasmacytic infiltration, obliterative phlebitis, and cholangitis with edema. Idiopathic duct-centric CP (IDCP) (n = 12) had neutrophil-predominant lobular inflammation, without phlebitis. On correlation of clinical and histologic diagnosis, 17 of 18 (94%) patients with alcohol-induced TCP had typical CP, and 25 of 27 (93%) with idiopathic TCP had LPSP or IDCP. LPSP and IDCP were indistinguishable clinically except for higher incidence of jaundice in LPSP (93% vs. 42%, P = 0.005). In idiopathic TCP no recurrence of symptoms was observed after resection (median follow-up 49 mo). Conclusions: Idiopathic TCP is clinically and histologically distinct from alcohol-induced TCP. It is unclear whether LPSP and IDCP, 2 unique patterns of histologic injury observed in idiopathic TCP, are part of the spectrum of the same disease or represent 2 or more different entities. Resection of mass prevents recurrence of symptoms in idiopathic TCP.
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页码:129 / 135
页数:7
相关论文
共 27 条
[1]  
Dehner LP, 1998, SEMIN DIAGN PATHOL, V15, P161
[2]   Non-alcoholic duct destructive chronic pancreatitis [J].
Ectors, N ;
Maillet, B ;
Aerts, R ;
Geboes, K ;
Donner, A ;
Borchard, F ;
Lankisch, P ;
Stolte, M ;
Luttges, J ;
Kremer, B ;
Kloppel, G .
GUT, 1997, 41 (02) :263-268
[3]   Sclerosing pancreato-cholangitis responsive to steroid therapy [J].
Erkelens, GW ;
Vieggaar, FP ;
Lesterhuis, W ;
van Buuren, HR ;
van der Werf, SDJ .
LANCET, 1999, 354 (9172) :43-44
[4]  
FORSMARK C, 2002, SLEISENGER FORDTRANS, V1, P943
[5]   Autoimmune pancreatitis: Radiologic findings in three histologically proven cases [J].
Furukawa, N ;
Muranaka, T ;
Yasumori, K ;
Matsubayashi, R ;
Hayashida, K ;
Arita, Y .
JOURNAL OF COMPUTER ASSISTED TOMOGRAPHY, 1998, 22 (06) :880-883
[6]   High serum IgG4 concentrations in patients with sclerosing pancreatitis. [J].
Hamano, H ;
Kawa, S ;
Horiuchi, A ;
Unno, H ;
Furuya, N ;
Akamatsu, T ;
Fukushima, M ;
Nikaido, T ;
Nakayama, K ;
Usuda, N ;
Kiyosawa, K .
NEW ENGLAND JOURNAL OF MEDICINE, 2001, 344 (10) :732-738
[7]   Sclerosing pancreato-cholangitis responsive to corticosteroid therapy: report of 2 case reports and review [J].
Horiuchi, A ;
Kawa, S ;
Hamano, H ;
Ochi, Y ;
Kiyosawa, K .
GASTROINTESTINAL ENDOSCOPY, 2001, 53 (04) :518-522
[8]  
Horiuchi A, 1996, AM J GASTROENTEROL, V91, P2607
[9]   ERCP features in 27 patients with autoimmune pancreatitis [J].
Horiuchi, A ;
Kawa, S ;
Hamano, H ;
Hayama, M ;
Ota, H ;
Kiyosawa, K .
GASTROINTESTINAL ENDOSCOPY, 2002, 55 (04) :494-499
[10]   Autoimmune pancreatitis as a new clinical entity - Three cases of autoimmune pancreatitis with effective steroid therapy [J].
Ito, T ;
Nakano, I ;
Koyanagi, S ;
Miyahara, T ;
Migita, Y ;
Ogoshi, K ;
Sakai, H ;
Matsunaga, S ;
Yasuda, O ;
Sumii, T ;
Nawata, H .
DIGESTIVE DISEASES AND SCIENCES, 1997, 42 (07) :1458-1468