[CIS PIDD] [cis-pidd] Unusual inflammatory disease

[Naides, Stanley J]

Consider B19 infection for the anemia and dyserythropoiesis.   Perhaps
also the arthritis.  Colitis would be unusual for B19, but worth a look
for the anemia and arthritis.

Stanley J. Naides, M.D., F.A.C.P., F.A.C.R. 
Medical Director, Immunology R&D | Interim Scientific Director,
Immunology R&D
Quest Diagnostics Nichols Institute | Immunology | 33608 Ortega Highway
| San Juan Capistrano, CA 92675 USA | phone +1.949.728.4578 | fax
+1.949.728.7852 | eFax +1.201.918.3297
Stanley.J.Naides at QuestDiagnostics.com | www.NicholsInstitute.com

-----Original Message-----
From: Verbsky, James [mailto:jverbsky at mcw.edu] 
Sent: Thursday, November 20, 2014 3:35 PM
To: CIS-PIDD
Subject: Re: [cis-pidd] Unusual inflammtory disease

Non consanguineous no family history

Sent from my iPhone

On Nov 20, 2014, at 5:14 PM, "Jason Raasch"
<jraasch at midwestimmunology.com<mailto:jraasch at midwestimmunology.com>>
wrote:

James, this may be neither here nor there, but anything interesting in
family history?

-J




Jason Raasch, MD

Midwest Immunology Clinic
15700 37th Ave N, Ste 110
Plymouth, MN 55446

TEL: (763) 577-0008
FAX: (763) 577-0192







On 11/20/14 4:19 PM, "Verbsky, James" wrote:
Hello all...we are stumped


6 month old AA boy presents with fevers, pseudoparalysis(wouldn't move
his legs) of lower extremities, serositis, high inflammatory markers,
hypoalbuminemia.

Found to have bone lesions in legs(biopsy non specific not cancer), knee
arthritis, and diffuse fascial fluid and edema in fascial planes
throughout, pleural effusions and peritoneal  ascites.

Also with diarrhea (first thought to be related to parecho virus but
hasn't improved).  Endoscopy showed predominantly acute inflammation in
the duodenum with flattened villi as well as acute colitis.  Currently
on TPN and cannot tolerate anything more than trophic feeds without
dumping syndrome.  Several infectious workups done and negative (except
for parecho virus).

Also very anemic...at first thought to be inflammatory, but is
transfusion dependent.  Marrow x2 showed few erythroid elements, lots of
myeloid elements, no leukemia, possible dyserythropoiesis.

Tried anakinra first...helped clinically with arthritis, moving better,
and feeling better.  No effect on GI.  Did not cure inflammation

WBC range from 15-37K.  ESR >100  CRP  CRP 20-25mg/dL(0-1.0 normal),
improved to 4 on anakinra but has stayed there since.

IgG of 1460  IgA 89 IgE 873.  Normal C3/C4

Lymphocyte subsets were essentially normal, but for whatever reason
several markers (CD3/TCR/CD20) showed poor staining on multiple
occasions with normal controls.  Staining improved when PBMCs were used
and washed (??? Not sure what that means, inhibitor?)

Normal lymphocyte subsets, normal CD11b/CD15/CD18 expression, DHR normal
(preactivated), Foxp3 detectable, CD25 present,  TLR testing normal (to
LPS), IL-10 suppression normal, responds to MDP (xIAP).

Was thinking Majeed syndrome, but fever syndrome testing normal except
for VUS in pyrin (waiting for report).  Started prednisone last week
without clear improvement.  Exome sent.(will check LRBA, CTLA4, STAT1,
IL10)

Cant put a dyserythropoietic anemia together with bowel disease and
acute inflammation.  Thinking autoimmune enteropathy (although pathology
says this looks different, will rescope)

Thoughts?

James W. Verbsky M.D./Ph.D.
Associate Professor of Pediatrics and Microbiology Medical College of
Wisconsin Milwaukee, WI
414-266-6701


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