CT and MRI features

Ali D. Karaosmanoglu, Naoki Takahashi, Dushyant V. Sahani

Research output: Chapter in Book/Report/Conference proceedingChapter

Abstract

Autoimmune pancreatitis (AIP) is a recently defined clinical entity. It is an uncommon disease with unique clinical and histological manifestations. It can be classified under the umbrella term of chronic pancreatitis and was first reported with the name of lymphoplasmacytic sclerosing pancreatitis with cholangitis in 1991. The term autoimmune pancreatitis was introduced in 1995. The clinical signs and symptoms mimic multiple diseases and early diagnosis is often difficult. The main pathologic abnormality is the infiltration of the pancreatic periductal areas with lymphocytes and plasma cells with subsequent destruction of the duct epithelium and venulitis [1]. Imaging plays a fundamental role in the diagnosis with some unique features that can be used to avoid a delayed diagnosis. Cross-sectional imaging can provide key findings to aid in the diagnosis and help avoid unnecessary testing and even surgery. In this chapter, we present the imaging findings associated with the pancreatic manifestations seen in patients with IgG4-related disease (IgG4-RD).

Original languageEnglish (US)
Title of host publicationAutoimmune (IgG4-Related) Pancreatitis and Cholangitis
PublisherSpringer New York
Pages145-155
Number of pages11
Volume9781441964304
ISBN (Electronic)9781441964304
ISBN (Print)1441964290, 9781441964298
DOIs
StatePublished - Feb 1 2013

Fingerprint

Pancreatitis
Cholangitis
Delayed Diagnosis
Chronic Pancreatitis
Plasma Cells
Signs and Symptoms
Names
Early Diagnosis
Epithelium
Immunoglobulin G
Lymphocytes

ASJC Scopus subject areas

  • Medicine(all)

Cite this

Karaosmanoglu, A. D., Takahashi, N., & Sahani, D. V. (2013). CT and MRI features. In Autoimmune (IgG4-Related) Pancreatitis and Cholangitis (Vol. 9781441964304, pp. 145-155). Springer New York. https://doi.org/10.1007/978-1-4419-6430-4_14

CT and MRI features. / Karaosmanoglu, Ali D.; Takahashi, Naoki; Sahani, Dushyant V.

Autoimmune (IgG4-Related) Pancreatitis and Cholangitis. Vol. 9781441964304 Springer New York, 2013. p. 145-155.

Research output: Chapter in Book/Report/Conference proceedingChapter

Karaosmanoglu, AD, Takahashi, N & Sahani, DV 2013, CT and MRI features. in Autoimmune (IgG4-Related) Pancreatitis and Cholangitis. vol. 9781441964304, Springer New York, pp. 145-155. https://doi.org/10.1007/978-1-4419-6430-4_14
Karaosmanoglu AD, Takahashi N, Sahani DV. CT and MRI features. In Autoimmune (IgG4-Related) Pancreatitis and Cholangitis. Vol. 9781441964304. Springer New York. 2013. p. 145-155 https://doi.org/10.1007/978-1-4419-6430-4_14
Karaosmanoglu, Ali D. ; Takahashi, Naoki ; Sahani, Dushyant V. / CT and MRI features. Autoimmune (IgG4-Related) Pancreatitis and Cholangitis. Vol. 9781441964304 Springer New York, 2013. pp. 145-155
@inbook{79826451c0564f2bb52c999ea43f2c51,
title = "CT and MRI features",
abstract = "Autoimmune pancreatitis (AIP) is a recently defined clinical entity. It is an uncommon disease with unique clinical and histological manifestations. It can be classified under the umbrella term of chronic pancreatitis and was first reported with the name of lymphoplasmacytic sclerosing pancreatitis with cholangitis in 1991. The term autoimmune pancreatitis was introduced in 1995. The clinical signs and symptoms mimic multiple diseases and early diagnosis is often difficult. The main pathologic abnormality is the infiltration of the pancreatic periductal areas with lymphocytes and plasma cells with subsequent destruction of the duct epithelium and venulitis [1]. Imaging plays a fundamental role in the diagnosis with some unique features that can be used to avoid a delayed diagnosis. Cross-sectional imaging can provide key findings to aid in the diagnosis and help avoid unnecessary testing and even surgery. In this chapter, we present the imaging findings associated with the pancreatic manifestations seen in patients with IgG4-related disease (IgG4-RD).",
author = "Karaosmanoglu, {Ali D.} and Naoki Takahashi and Sahani, {Dushyant V.}",
year = "2013",
month = "2",
day = "1",
doi = "10.1007/978-1-4419-6430-4_14",
language = "English (US)",
isbn = "1441964290",
volume = "9781441964304",
pages = "145--155",
booktitle = "Autoimmune (IgG4-Related) Pancreatitis and Cholangitis",
publisher = "Springer New York",

}

TY - CHAP

T1 - CT and MRI features

AU - Karaosmanoglu, Ali D.

AU - Takahashi, Naoki

AU - Sahani, Dushyant V.

PY - 2013/2/1

Y1 - 2013/2/1

N2 - Autoimmune pancreatitis (AIP) is a recently defined clinical entity. It is an uncommon disease with unique clinical and histological manifestations. It can be classified under the umbrella term of chronic pancreatitis and was first reported with the name of lymphoplasmacytic sclerosing pancreatitis with cholangitis in 1991. The term autoimmune pancreatitis was introduced in 1995. The clinical signs and symptoms mimic multiple diseases and early diagnosis is often difficult. The main pathologic abnormality is the infiltration of the pancreatic periductal areas with lymphocytes and plasma cells with subsequent destruction of the duct epithelium and venulitis [1]. Imaging plays a fundamental role in the diagnosis with some unique features that can be used to avoid a delayed diagnosis. Cross-sectional imaging can provide key findings to aid in the diagnosis and help avoid unnecessary testing and even surgery. In this chapter, we present the imaging findings associated with the pancreatic manifestations seen in patients with IgG4-related disease (IgG4-RD).

AB - Autoimmune pancreatitis (AIP) is a recently defined clinical entity. It is an uncommon disease with unique clinical and histological manifestations. It can be classified under the umbrella term of chronic pancreatitis and was first reported with the name of lymphoplasmacytic sclerosing pancreatitis with cholangitis in 1991. The term autoimmune pancreatitis was introduced in 1995. The clinical signs and symptoms mimic multiple diseases and early diagnosis is often difficult. The main pathologic abnormality is the infiltration of the pancreatic periductal areas with lymphocytes and plasma cells with subsequent destruction of the duct epithelium and venulitis [1]. Imaging plays a fundamental role in the diagnosis with some unique features that can be used to avoid a delayed diagnosis. Cross-sectional imaging can provide key findings to aid in the diagnosis and help avoid unnecessary testing and even surgery. In this chapter, we present the imaging findings associated with the pancreatic manifestations seen in patients with IgG4-related disease (IgG4-RD).

UR - http://www.scopus.com/inward/record.url?scp=84930335917&partnerID=8YFLogxK

UR - http://www.scopus.com/inward/citedby.url?scp=84930335917&partnerID=8YFLogxK

U2 - 10.1007/978-1-4419-6430-4_14

DO - 10.1007/978-1-4419-6430-4_14

M3 - Chapter

AN - SCOPUS:84930335917

SN - 1441964290

SN - 9781441964298

VL - 9781441964304

SP - 145

EP - 155

BT - Autoimmune (IgG4-Related) Pancreatitis and Cholangitis

PB - Springer New York

ER -