A Tale of Two “States:” A Penny for Your Thoughts

A 36-year-old female, diagnosed as ulcerative colitis and primary sclerosing cholangitis [Figure 1], was on intermittent mesalamine, prednisolone, and ursodeoxycholic acid since 2013. She presented in 2023 with weight loss, pruritus, bleeding per rectum, and fatigue. She had no history of abdominal pain, fever, or jaundice. Review of previous records showed persistent elevation of serum alkaline phosphatase (159–455 IU/L) and gamma-glutamyl transferase (98–505 IU/L), with normal bilirubin, albumin, and transaminases. Complete blood counts showed leukocytosis (range: 12,600–29,740 Mm3), raised eosinophil count (23%–65%), absolute eosinophil count (624 cells/mm3 to 20,084 cells/mm3), and thrombocytosis (540–819 × 103/µL). Autoimmune workup was positive for ANA 1:100 and perinuclear anti-neutrophil cytoplasmic antibody. Colonoscopy showed mild erythema in the rectum and sigmoid colon. Biopsy showed increased eosinophils in lamina propria (20–30/high-power field) with focal cryptitis and crypt distortion. Bone marrow study showed erythroid suppression and myeloid hyperplasia, with increase in eosinophils and its precursors [Figure 2a and b]. Eosinophilia FISH Leukemia Panel (PDGFRA, PDGGFRB, FGFR1, and CBFB) was negative. Final diagnosis: Idiopathic hypereosinophilic syndrome, eosinophilic colitis, and likelihood of eosinophilic sclerosing cholangitis.[1,2] The patient is currently on steroids, colitis is in remission, eosinophils are normal (3%–4%), and liver biochemistry is normal.Figure 1: MRCP – classical features (large and small duct)Figure 2: (a) Colonic biopsy showing increase of sclerosing cholangitis in eosinophils per high-power field. (b) Bone marrow aspirate showing numerous eosinophilsDeclaration of patient consent The authors certify that they have obtained all appropriate patient consent forms. In the form, the patient has given her consent for her images and other clinical information to be reported in the journal. The patient understands that her name and initials will not be published and due efforts will be made to conceal identity, but anonymity cannot be guaranteed. Financial support and sponsorship Nil. Conflicts of interest There are no conflicts of interest.

Authors

Publication Details

Journal
Gastroenterology Hepatology and Endoscopy Practice
Published
2025-03-20
DOI
https://doi.org/10.4103/ghep.ghep_40_24
Primary Topic
IgG4-Related and Inflammatory Diseases
Type
article
Field-Weighted Citation Impact
0.00
Controls
|||
ALL TIME
JAN
FEB
MAR
APR
MAY
JUN
JUL
AUG
SEP
OCT
article

A Tale of Two “States:” A Penny for Your Thoughts

Mayank Jain, Jayanthi Venkataraman
Gastroenterology Hepatology and Endoscopy Practice
IgG4-Related and Inflammatory Diseases
article

A Tale of Two “States:” A Penny for Your Thoughts

Mayank Jain, Jayanthi Venkataraman
article en

Abstract

A 36-year-old female, diagnosed as ulcerative colitis and primary sclerosing cholangitis [Figure 1], was on intermittent mesalamine, prednisolone, and ursodeoxycholic acid since 2013. She presented in 2023 with weight loss, pruritus, bleeding per rectum, and fatigue. She had no history of abdominal pain, fever, or jaundice. Review of previous records showed persistent elevation of serum alkaline phosphatase (159–455 IU/L) and gamma-glutamyl transferase (98–505 IU/L), with normal bilirubin, albumin, and transaminases. Complete blood counts showed leukocytosis (range: 12,600–29,740 Mm3), raised eosinophil count (23%–65%), absolute eosinophil count (624 cells/mm3 to 20,084 cells/mm3), and thrombocytosis (540–819 × 103/µL). Autoimmune workup was positive for ANA 1:100 and perinuclear anti-neutrophil cytoplasmic antibody. Colonoscopy showed mild erythema in the rectum and sigmoid colon. Biopsy showed increased eosinophils in lamina propria (20–30/high-power field) with focal cryptitis and crypt distortion. Bone marrow study showed erythroid suppression and myeloid hyperplasia, with increase in eosinophils and its precursors [Figure 2a and b]. Eosinophilia FISH Leukemia Panel (PDGFRA, PDGGFRB, FGFR1, and CBFB) was negative. Final diagnosis: Idiopathic hypereosinophilic syndrome, eosinophilic colitis, and likelihood of eosinophilic sclerosing cholangitis.[1,2] The patient is currently on steroids, colitis is in remission, eosinophils are normal (3%–4%), and liver biochemistry is normal.Figure 1: MRCP – classical features (large and small duct)Figure 2: (a) Colonic biopsy showing increase of sclerosing cholangitis in eosinophils per high-power field. (b) Bone marrow aspirate showing numerous eosinophilsDeclaration of patient consent The authors certify that they have obtained all appropriate patient consent forms. In the form, the patient has given her consent for her images and other clinical information to be reported in the journal. The patient understands that her name and initials will not be published and due efforts will be made to conceal identity, but anonymity cannot be guaranteed. Financial support and sponsorship Nil. Conflicts of interest There are no conflicts of interest.

Gastroenterology Hepatology and Endoscopy PracticeVol. 5(2)
Openalex Percentile: Top 92%
IgG4-Related and Inflammatory Diseases
AI Navigator

Ask Laika to Summarize, Analyze, and Connect papers live on the map.

Summarize Papers & Methodologies

Extract key findings, datasets, and comparative methods across publications.

Benchmark Rankings & Visual Analytics

Rank top research institutions, authors, funders, topics, and journals by Field-Weighted Citation Impact (FWCI) and paper volume with instant charts.

Connect Distant Disciplines

Bridge topological clusters on the map to find hidden collaborative intersections.