[CIS-PAGID] Infant with lymphopenia, elevated IgG and IgM, bony changes, PCP

[Verbsky, James]

Tamara

The lack of fever and relative low ferritin doesn't sound much like HLH.  NK dysfunction is supportive..but there are lots of situations that cytotoxicity can be abnormal.  This should be repeated.

Since IL-2Ra is detectable and elevated..this argues against CD25 deficiency (although could still be non functional).  Is there any diarrhea/bowel disease??  The CMV status could be consistent with IL-2 signaling defectws.  Stat5??  T cell mitogens will be helpful.

IL-1RA deficiency should give you thromobcytosis..and the putstular rash is striking and somewhat hard to miss.  At least in our patient..there was widespread severe osteopenia with specific lytic lesions..your description of bone isnt consistent.  However..if you want to rule this out give the kid anakinra for a couple of days and they will be cured.

Hyper IgE (without the IgE)??

I like the histiocytosis angle..I found cases of histiocytic panniculitis..they are old but sound like a variant of LCH..Dr Bleesing and others can certainly comment on these issues better than I

Good luck

James

 


James W. Verbsky M.D./Ph.D. 
Assistant Professor of Pediatrics and Microbiology and Molecular Genetics
Medical College of Wisconsin 
Children's Corporate Center 
Pediatric Rheumatology, Suite C465 
9000 W. Wisconsin Ave., PO Box 1997 
Milwaukee, WI 53201-1997 
(work) 414-266-6585 
(pager) 414-907-3134 
(fax) 414-266-6695 
jverbsky at mcw.edu 
verbskyj at yahoo.com


-----Original Message-----
From: pagid-bounces at list.clinimmsoc.org [mailto:pagid-bounces at list.clinimmsoc.org] On Behalf Of Tamara Pozos
Sent: Thursday, December 02, 2010 9:46 AM
To: Jack.Bleesing at cchmc.org; pagid at list.clinimmsoc.org
Subject: Re: [CIS-PAGID] Infant with lymphopenia, elevated IgG and IgM, bony changes, PCP

Thanks for thinking about her with me, Jack.  

All of the numbers are down in the longer version of the case, but HLH data in particular:

 lack of fever
 lack of hemophagocytosis on 2 bone marrow biopsies
suggestive:	
Interleukin-2 Receptor >6500 U/mL & (H)
Lytic Unit, NK Function 2.6 & (L) (Ref. Range 3.2 - 95.8) Ferritin 230-260-310 (3 values over time) Fibrinogen 107-70-133 Triglycerides 306-687-651

lytic lesions were not seen on her bones, but LCH has been on the list.


thanks again, grateful for your insights Tam


Tamara Pozos, MD PhD
Pediatric Infectious Diseases and Immunology Children's Hospitals and Clinics of Minnesota Mail Stop 70-504 Garden View Building, 5th Floor
345 Smith Avenue North
St. Paul, MN  55102
tamara.pozos at childrensmn.org
651-220-6444 (office)

>>> "Jack Bleesing" <Jack.Bleesing at cchmc.org> 12/02/10 8:33 AM >>>

Sticking to HLH and such: what is the ferritin and how high is sIL2R?

Bone lesions: consider LCH (which can have overlap with HLH - systemic involvement).

Regards,

Jack
-----Original Message-----
From: "Tamara Pozos" <Tamara.Pozos at childrensmn.org>
To:  <pagid at list.clinimmsoc.org>

Sent: 12/1/2010 7:02:38 PM
Subject: [CIS-PAGID] Infant with lymphopenia, elevated IgG and IgM, bony changes, PCP

Hello all - thanks in advance for thinking about this concerning patient with me.  Below are a short version of the case, my questions, and then a more detailed summary.

3-month-old Laotian girl with thrombocytopenia, splenomegaly, failure to thrive, resolved complex rash (panniculitis on two biopsies, mild eczema), abnormal neuroimaging, bony abnormalities.
Immunologic abnormalities: lymphopenia (~2000, lower after steroids),
elevated IgM at 327, elevated IgG >1000;    IgE normal.  
NO fever, no thrush, no diarrhea.  Soon after hospitalization she developed PCP, now intubated in the ICU, clinically improving on steroids and TMP/SMX (and other broad antimicrobials).  HIV negative.

my differential for now:
High concern for BMT-requiring diagnoses: SCID, hyper IgM.  
Eczematous rash was very mild, normal IgE/eos, lymphopenic,  IgG and IgM high, so not classic for OS.  
There are suggestive data in support of HLH as well (very high sIL2R, low NK function), but lacking some classic features (like fever or
hemophagocytosis) - and recognizing that severe immune deficiency and HLH are not mutually exclusive diagnoses.
Given bony and immune abnormalities, RMRP mutation possible (one recent report of a Thai child with cartilage-hair-hypoplasia).  
Our patient's rash did not evolve to pustules, and her bony changes, per radiology, are less consistent with those reported for DIRA.  
JMML still possible per oncology, but less likely.   

Questions:
Is further pursuing hyperIgM or RMRP mutations indicated now?  CD25 deficiency? Other favored diagnoses?
Has anyone seen a similar case with panniculitis as the initial rash? 
Are the features of HLH strong enough to consider etoposide as well as continuing steroids (she is clinically improving with steroids alone)? 


Any other diagnostic or treatment thoughts from your collective experience are very welcome.  more details are below.

Thank you very much for your time,

Tamara Pozos, MD PhD
Pediatric Infectious Diseases and Immunology Children's Hospitals and Clinics of Minnesota St. Paul, MN tamara.pozos at childrensmn.org
651-220-6444 (main office) - 6293 (personal line)

 



Summary of case:
Born at term to a 33-year-old prima gravida.  FHx neg for immunodeficiency. No cosanguinity known.
1st week of life nodular/plaque rash on her arms and legs - biopsy:
lobular panniculitis
1.5 months of life, splenomegaly first noted, thrombocytopenia (95K), anemia (7), monocytosis also noted but has not progressed. Positive alpha thal trait. workup for neonatal lupus and malignancy negative inc NB and JMML: normal marrow.
Developed mild dry eczematous skin over face, chest and arms, never became pustules. Improved during hospitalization with moistCMV PCR + for 4K copies. Head ultrasound showed mild dilatation of lateral ventricles and subarachnoid space, no focal lesions, calcifications or hemorrhage.  Retinas and hearing normal.  Other infectious diseases testing negative.

She has not been febrile throughout, except one temp 39 on evening of first marrow biopsy.  To her parents she was acting and developing normally. 

Sent to our ID clinic to discuss CMV, found to have diffuse, not dramatic, lymphadenopathy, larger spleen, newly enlarged liver, and
falling off growth curve -   eczematous rash very mild.   Admitted for
evaluation.
Plt 75, AST/ALT normal.  Repeat CMV PCR revealed no viremia, prior to antivirals, but given a +CMV IgM and immunologic abnormalities ganciclovir started.
HIV negative (antibodies and DNA and RNA PCRs) 

Immunologic eval:
Elevated IgG 1280 (sub 2-4 normal) and IgM 181.   IgA and IgE normal. 
Eos normal throughout.

ALC low at 2200 (5000-7900)
CD3+ 75%  absolute 1650
CD3+ a/b+ 70%, g/d+ 6%
CD3+ HLA-DR+ 23 % (0 - 8)
CD3+CD4+ 45% absolute 990 (1200-4500)
CD3+CD8+ 25%  absolute 550
DNTs 0.6% abs 13

CD19+ 13%  abs 286
CD16+56+ 11%  abs 1540

Skeletal survey: abnormal flaring and cupping of distal metaphyses of
the bilateral radii, ulnas, femurs, tibia. Distal metaphyses of the left
metatarsals have a somewhat cupped appearance. Relatively symmetric
increased periostitis along the anterior aspect of the bilateral tibias,
which may be physiologic.  No focal geographic lucencies to suggest
Langerhans cell histiocytosis. 

MRI of head revealed expansion of extra-axial spaces, possibly
consistent with cerebral atrophy given microcephaly (Head size was
normal at 2 months, but stopped growing). 

Clinical evolution - Despite lack of fever and lack of
hemophagocytosis on 1st bone marrow biopsy, labs for HLH sent and
suggestive:	
Interleukin-2 Receptor >6500 U/mL & (H)
Lytic Unit, NK Function 2.6 & (L) (Ref. Range 3.2 - 95.8)
Ferritin 230-260-310 (3 values over time)
Fibrinogen 107-70-133
Triglycerides 306-687-651

Eczematous type rash completely resolved (prior to steroids).  
Worsening respiratory status, O2 need - positive PCP on bronchoscopy
- on steroids and TMP/SMX, intubated in the ICU.  
Panniculitis lesions, splenomegaly and thrombocytopenia improving on
steroids.

LP: 12 WBC, 27 RBC, glucose 29, protein 70.  Cytospin showed no
hemophagocytosis. 
Repeat bone marrow was again negative for hemophagocytosis.

Current status: weaning towards extubation.  
After 5 days of Decadron, lymphocyte numbers decreasing.  IgM
increasing further.
IgG 1170 (age 15 weeks. Nl 169-536)   IgM 327 ( 23-85).   A and M still
normal - IgA 24, IgE 6.7. 

ALC 1155
CD3+ 61%,   abs 705
DR+ activated % 16%
CD4+ 32%   abs 370
CD8+ 26%   abs 300

CD19+ 31%  abs 358
CD16+56+ 8%  abs 92

In terms of possible maternal engraftment: decreased CD8+ CD45RA (68%);

majority of Tcells are not RO+ but at upper limits of normal
(CD4+CD45RO 21%, CD8+CD45RO 13%). 

Mitogen and antigen proliferative responses pending, but also sent
after steroids started.





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