[PAGID] two questions on enteritis

YaeJean Kim yaejeankim at skku.edu
Sat Jun 27 06:40:51 EDT 2009


Thanks, Troy and others,



We are actually repeating the test since the evaluation was done last year.
Mom is kind of slow or somewhat retarded (mildly), but communication is
reasonable.



Last year when he was 8 months, CD25+ cells were observed. For CGD, NBT test
was done which was normal. We did not do FOXP3 flow, CD45RA or CD45RO flow
and I will repeat those tests.



He has eczema and rash but no other autoimmune feature at least. No anemia,
no thrombocytopenia, no liver problems.

We will try to do the sequencing again with all the other tests you
mentioned.

Below is the flow result from last year for cell numbers.



- CBC & Diff. count (08.11.2008)

WBC count : 8,310/ul

Lymphocyte % : 64%

Lymphocyte count : 5,320/ul

- Result

=================================

Parameter Test value

(MoAb) % Count(/ul)

---------------------------------

T (CD3) 74 3,950

T4 (CD4) 35 1,860

T8 (CD8) 37 1,970

T4/T8 ratio 0.95

B (CD19) 17 900

NK (CD16+56) 4 210

---------------------------------



Thanks a lot for your comments and I will update the progress.



YaeJean

_____

From: pagid-bounces at list.clinimmsoc.org
[mailto:pagid-bounces at list.clinimmsoc.org] On Behalf Of Torgerson, Troy
Sent: Friday, June 26, 2009 8:21 AM
To: pagid at list.clinimmsoc.org
Subject: Re: [PAGID] two questions on enteritis



YaeJean,



IPEX is certainly a good initial thought given his symptoms but I would
include a couple of other disorders:

First, for IPEX: Has he had eczema or other rash? Has he had other
autoimmunity as well (hemolytic anemia, thrombocytopenia, liver disease,
etc.)? Most of the pts with FOXP3 mutations have other autoimmune
manifestations in addition to the enteropathy, eczema, and endocrinopathy.
Have you been able to get flow cytometry done to see if he has FOXP3+ cells
in his CD4+ population, would also look at CD25 expression by flow to make
sure it is there (see James’ comment)? When they sequenced FOXP3, do you
know what they sequenced and how much of the gene they looked at? About 5%
of the mutations we have identified are in non-coding regions of the gene
(polyadenylation site or upstream non-coding region). If they sequenced
genomic DNA did they look at all of the exon/intron junctions to rule out a
splicing mutation or did they sequence cDNA?



Second, Leaky SCID: Some Leaky SCID/Omenn or maternally engrafted SCID
patients can look a lot like IPEX. Pts with IPEX can get infections for
sure but pneumonias are not all that common and “frequent” infections are
not all that common. What are the T/B/NK numbers? Are they his T/B/NK
cells or his mom’s? Do his T cells proliferate to mitogens/antigens? Do
you know whether his T cells are mostly CD45RA+ (naïve) or CD45RO+ (mature)?
– leaky SCID’s & maternally engrafted SCID’s are usually very skewed to
CD45RO+. Are his parents consanguineous?



Third, CGD: Incidence of IBD/IBD-like symptoms is very high in CGD and we
recently saw an infant here in Seattle with initial presentation of early
onset “Crohn’s” disease with granulomatous lesions on biopsy that has X-CGD.
Pneumonia also common in CGD. Would check neutrophil oxidative burst as
this would dramatically alter the therapeutic approach.



Best,



TT



Troy R. Torgerson, MD PhD



Assistant Professor, Pediatric Immunology/Rheumatology

University of Washington, Department of Pediatrics



Co-Director, Immunology Diagnostic Laboratory

Center for Immunity and Immunotherapies

Seattle Children’s Research Institute

1900 9th Ave., C9S-7

Seattle, WA 98101-1305



Tel: (206) 987-7450

Fax: (206) 987-7310



Email: Troy.Torgerson at seattlechildrens.org



_____

From: pagid-bounces at list.clinimmsoc.org
[mailto:pagid-bounces at list.clinimmsoc.org] On Behalf Of YaeJean Kim
Sent: Thursday, June 25, 2009 2:46 PM
To: pagid at list.clinimmsoc.org
Subject: [PAGID] two questions on enteritis



Dear all,



I am YaeJean Kim who attended the 2007 PID summer school while I was a
fellow in Seattle and now am relocated to Seoul, Korea.



I see a patient in my institute and have questions as below.



This is a now 18 month boy who is suspected for IPEX or IPEX like syndrome.
He has had intractable diarrhea, recurrent infections including pneumonia
and anal infection, fistula, hypothyroidism (only endocrinopathy
manifestiation he has) since age of 1 month. His brother died too with
similar features.



He was initially presented with failure to thrive. Intestinal biopsy (at the
age of 7 mo) was suspected for IPEX but FOXP3 mutation was not observed.
Because of severe anal fistula, he received cecostomy. He is now on
azathioprine by our GI guy who is the main doctor for him. He still seems to
have frequent infection with fevers and get hospitalized for antibiotics. Do
you have any suggestions? Or should we repeat the test? All the tests were
done about 10 months ago.



I would appreciate any feedback. Thanks a lot.





Jean



--------------------------------------------



YaeJean Kim, MD



Assistant Professor

50 Ilwon-dong Gangnam-gu

Division of Infectious Diseases

Department of Pediatrics

Samsung Medical Center

Sunggyungwan University

Seoul, 135-710

South Korea

tel) 82-2-3410-3539, 0987

fax) 82-2-3410-0043

yaejeankim at skku.edu



Children's Hospital and Regional Medical Center is now Seattle Children's.
CONFIDENTIALITY NOTICE: This e-mail message, including any attachments, is
for the sole use of the intended recipient(s) and may contain confidential
and privileged information protected by law. Any unauthorized review, use,
disclosure or distribution is prohibited. If you are not the intended
recipient, please contact the sender by reply e-mail and destroy all copies
of the original message.

-------------- next part --------------
An HTML attachment was scrubbed...
URL: <http://seven.pairlist.net/mailman/private/pagid/attachments/20090627/12079c63/attachment-0001.html>


More information about the PAGID mailing list