Hyperimmunoglobulin E syndrome (Job's syndrome) with acute coccidioidal meningoencephalitis

Authors: Sean Stanga, M.D.; Maria Victoria Dajud, M.D., Blank Children's Hospital
Reviewer: V. Dimov, M.D., Allergist/Immunologist and Assistant Professor at University of Chicago

A 4-year-old female was admitted on transfer from a regional medical center for symptoms of nausea, vomiting, dehydration, and complaints of headache and visual changes for approximately four days. Her symptoms had progressively worsened over time and the patient was admitted for suspected meningitis.

Past medical history (PMH)

Past medical history was significant for recurrent upper respiratory infections as well as sinus and skin infections, most notably eczema herpeticum. Previous metabolic and immunologic workup for her symptoms was significant only for an elevated immunoglobulin E, 805 (nl. 0-230 U/mL), and no definitive diagnosis was established at that time.

Medications

No medications.

Allergies

No allergies.

Physical Examination

Fever, nuchal rigidity and photophobia. Dry mucosal membranes and mild tachycardia. The rest of the physical examination was unremarkable.

What is the most likely diagnosis?

Likely bacterial vs. viral meningitis.

What tests would you suggest?

CBC with differential
Comprehensive Metabolic Panel
Urinalysis
Blood Culture
Lumbar Pucture with cell count, differential, culture for bacteria and HSV PCR
Chest X-ray

What happened?

On admission, her WBC count was 12,970/mm3 with 78.5% neutrophils, 12.6% lymphocytes, 6.8% monocytes, 1.9% eosinophils. Hemoglobin, hematocrit, platelets, comprehensive metabolic panel, and urinalysis were all within normal limits. Lumbar puncture was performed which yielded cloudy spinal fluid with 623 white blood cells, and 2 red blood cells. Differential showed 14% neutrophils, 55% lymphocytes, 9% monocytes, and 18% eosinophils. CSF glucose 53, protein 43.2, and Gram stain was negative for microorganisms. Blood culture was negative. Chest x-ray and KUB were normal. CT performed at the outlying regional medical center was negative for any acute intracranial process. HSV PCR along with spinal fluid cultures were obtained and sent.

The patient was initially started on intravenous ceftriaxone for bacterial coverage and acyclovir for possible herpetic meningoencephalitis. On the second day of admission, the patient experienced several simultaneous tonic/clonic seizures that resolved with IV phenytoin. MRI of the brain revealed a small area of infarction within the left basal ganglia and the right superior cerebellar hemisphere. The patient was started on oxycarbazepine for seizure prophylaxis. Immunoglobulin and complement titers were sent. On day three of admission, the patient awoke with severe lethargy, bilateral lower extremity spasticity, right eye ptosis, horizontal nystagmus, and gross left-sided hemiplegia. Repeat MRI demonstrated very large infarcts in the left and right basal ganglia and the right temporal lobe not previously visualized. Blood cultures revealed no growth and HSV PCR was found to be negative on the third day. Immunoglobulin titers revealed an immunoglobulin E of 9147 (nl. 0-230 U/mL). Immunoglobulins A, G, M and complement C3, C4 were within normal limits.

What happened next?

Out of concern for a fungal infectious etiology, the patient was immediately transferred to a tertiary intensive care unit for infectious disease consult. The patient was started on intravenous voriconazole. Further workup and repeat lumbar puncture demonstrated CSF that grew Coccidioides immitus and antifungal therapy was switched to Amphotericin B. The patient recovered well after a prolonged hospital stay and suffered minimal deficits from the acute episodes of stroke. She was discharged on long term fluconazole therapy with extensive rehabilitation therapy in progress.

Final diagnosis

Hyperimmunoglobulin E syndrome (Job's syndrome) with acute coccidioidal meningoencephalitis.

What did we learn from this case?

While the most common source of CNS infection is dissemination from a primary pulmonary infection, our patient in question never manifested any respiratory symptoms or significant radiographic evidence of lung involvement. Her CNS infection likely was the result of a disseminated skin infection given her longstanding history of dermatitis. This patient had an underlying hyperimmunoglobulin E disease pathology which predisposed her to multiple superficial and systemic fungal infections. The fact that her underlying susceptibility to fungemia was not elicited until after severe CNS infection with an invasive fungal pathogen demonstrates the importance of obtaining immunoglobulin titers early in the course of an illness if an immunodeficiency is suspected.

References

1. Gottfredsson M, Perfect JR. Fungal meningitis. Semin Neurol 2000;20:307-322
2. Bronnimann DA, Adam RD, Galgiani JN, et al. Coccidioidomycosis in the acquired immunodeficiency syndrome. Ann Intern Med 1987;106:372-379
3. Chiller TM, Galgiani JN, Stevens DA. Coccidioidomycosis. Infect Dis Clin North Am 2003;17:41-57, viii
4. Johnson RH, Einstein HE. Coccidioidal meningitis. Clin Infect Dis 2006;42:103-107
5. Ragland AS, Arsura E, Ismail Y, Johnson R. Eosinophilic pleocytosis in coccidioidal meningitis: frequency and significance. Am J Med 1993;95:254-257
6. Beard JS, Benson PM, Skillman L. Rapid diagnosis of coccidioidomycosis with a DNA probe to ribosomal RNA. Arch Dermatol 1993;129:1589-1593
7. Kleinschmidt-DeMasters BK, Mazowiecki M, Bonds LA, Cohn DL, Wilson ML. Coccidioidomycosis meningitis with massive dural and cerebral venous thrombosis and tissue arthroconidia. Arch Pathol Lab Med 2000;124:310-314
8. de Carvalho CA, Allen JN, Zafranis A, Yates AJ. Coccidioidal meningitis complicated by cerebral arteritis and infarction. Hum Pathol 1980;11:293-296
9. Williams PL, Johnson R, Pappagianis D, et al. Vasculitic and encephalitic complications associated with Coccidioides immitis infection of the central nervous system in humans: report of 10 cases and review. Clin Infect Dis 1992;14:673-682
10. Antony SJ, Jurczyk P, Brumble L. Successful use of combination antifungal therapy in the treatment of coccidioides meningitis. J Natl Med Assoc 2006;98:940-942
11. Capilla J, Clemons KV, Sobel RA, Stevens DA. Efficacy of amphotericin B lipid complex in a rabbit model of coccidioidal meningitis. J Antimicrob Chemother 2007;60:673-676
12. Clemons KV, Sobel RA, Williams PL, Pappagianis D, Stevens DA. Efficacy of intravenous liposomal amphotericin B (AmBisome) against coccidioidal meningitis in rabbits. Antimicrob Agents Chemother 2002;46:2420-2426
13. Li RK, Ciblak MA, Nordoff N, Pasarell L, Warnock DW, McGinnis MR. In vitro activities of voriconazole, itraconazole, and amphotericin B against Blastomyces dermatitidis, Coccidioides immitis, and Histoplasma capsulatum. Antimicrob Agents Chemother 2000;44:1734-1736
14. Proia LA, Tenorio AR. Successful use of voriconazole for treatment of Coccidioides meningitis. Antimicrob Agents Chemother 2004;48:2341
15. Sorensen KN, Sobel RA, Clemons KV, et al. Comparative efficacies of terbinafine and fluconazole in treatment of experimental coccidioidal meningitis in a rabbit model. Antimicrob Agents Chemother 2000;44:3087-3091
16. Tucker RM, Galgiani JN, Denning DW, et al. Treatment of coccidioidal meningitis with fluconazole. Rev Infect Dis 1990;12 Suppl 3:S380-389
17. Tucker RM, Williams PL, Arathoon EG, et al. Pharmacokinetics of fluconazole in cerebrospinal fluid and serum in human coccidioidal meningitis. Antimicrob Agents Chemother 1988;32:369-373
18. Kamberi P, Sobel RA, Clemons KV, et al. Comparison of itraconazole and fluconazole treatments in a murine model of coccidioidal meningitis. Antimicrob Agents Chemother 2007;51:998-1003
19. Saitoh A, Homans J, Kovacs A. Fluconazole treatment of coccidioidal meningitis in children: two case reports and a review of the literature. Pediatr Infect Dis J 2000;19:1204-1208

Published: 12/07/2009
Updated: 12/07/2009

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Eosinophilic gastrointestinal disorder (EGID)

Author: S. Randhawa, M.D., Allergist/Immunologist and Assistant Professor at LSU (Shreveport) Department of Allergy and Immunology
Reviewer: V. Dimov, M.D., Allergist/Immunologist and Assistant Professor at University of Chicago

A 3-year old Caucasian boy with h/o severe anemia (hemoglobin 6 mg/dL) and hemoccult positive stools was admitted to the hospital. He was previously admitted 6 months ago with hemoglobin (Hb) 1.9 mg/dL, transfused, and a GI endoscopy showed a colonic polyp. The patient was started on iron therapy and the Hb improved but was never normal. According to the mother, he had no symptoms of bleeding. The patient’s stool has been black since he was started on iron.

Medications

Iron syrup.

Family and social history

Non contributory.

Birth History: he was born at 40 week gestation without any problems. Immunizations are up-to-date. Diet: Table food. Eats everything. The patient is developmentally appropriate for age.

Physical examination

Vital signs: Temp. 98.1, HR 112 bpm, RR 6, BP 92/58 mm Hg.
Wt 13.8 Kg.
HEENT: External ears normal. Canals clear. TM's normal. Nares normal. Septum midline. Oropharynx clear. Neck: supple, no adenopathy.
CVS: RRR, normal S1/S2, no m/r/g.
Chest: CTA (B).
Abdomen: Soft, Non tender BS +ive.
Extremities: no c/c/e.
Skin: color, texture, turgor normal. No rashes or lesions.

What laboratory tests would you suggest at this point?

CBCD
CMP
ESR
Stool O & P
Stool occult blood
TSH
UA
Blood cultures

Laboratory results

CBCD
WBC – 10.8
Hb – 7.3
Hct – 26.1
MCV- 68
Platelets- 194
Neutrophils - 30%
Lymphocytes - 49%
Monocytes – 4.3%
Eosinophils – 15.9% (1730)
Basophils - 1.6% (170)

CMP
Na - 138
K - 4.2
HCO3 24
BUN 26
Cr 1.1
Bilirubin Normal
AST 22
ALT 18
Ca Normal
Glucose 114
Total Protein 4.5 (low)
Albumin 2.1 (Low)

UA
Specific gravity – 1.020
pH - 5
Protein - None
Glucose - None
Ketone - None
Bilirubin - None
Blood - None
Nitrite - Negative
Leukocyte - Negative
Urobilinogen - None

TSH – 3.6
Stool occult blood - positive
Blood cultures negative
Ova & Parasites - negative
Stool Ova & Parasite
ESR – Within normal limits

The treatment team performed additional tests listed below:

Sweat Chloride test - negative
HIV: ELISA - negative, Western Blot - negative, PCR - no RNA copies identified.
Flow cytometry – Within normal limits

Radiology tests:

CXR - Within normal limits
CT Chest - Within normal limits.
CT abdomen - Within normal limits except for 1.7 cm intraluminal defect seen in the proximal jejunum without bowl dilatation.

Diagnostic procedures performed:

Sputum cytology - Within normal limits.
Pulmonary function testing - Within normal limits.
Upper Endoscopy – Showed signs of inflammation in esophagus, stomach and proximal deudenum. Biopsies were taken which showed an abundance of eosinophils (more than 50 per hpf) in the submucosa.
Colonoscopy - Showed patchy inflammation in the colon. Biopsies showed an infiltration of eosinophils in the submucosa.

Serological testing:

ANA – Negative
RA - Negative

RAST to food allergens:

Chicken - Class 0/1
Egg Class - 2
Fish Class - 0
Milk Class - 2
Soybean Class - 0
Wheat Class - 2

Thyroid antibodies
Anti thyroglobulin Ab – Negative
Anti peroxidase Ab – Negative
Anti microsomal Ab - Negative

Immunoglobulins

Total IgG - Within normal limits
IgG Subclasses (IgG1-4) – Within normal limits
Total IgA - Within normal limits
Total IgM – Within normal limits
Total IgE - 73

Food allergen skin testing - negative to Almond, Apple, Banana, Beef, Celery, Coconut, Corn, Cottonseed, Egg, Fish, Lobster, Milk, Pecan, Pea nut, Soybean, Shrimp, Walnut, Wheat.

DTH
Tetanus – Normal Response
PPD - Normal Response
Trichophyton - Normal Response
Candida - Normal Response

Delayed-type hypersensitivity (DTH) response

The standardized DTH test includes Candida, tetanus, mumps, and TB. Trichophyton is also commonly used. However, the only FDA-approved reagents for DTH are PPD, Candida and mumps.

Final Diagnosis

Eosinophilic gastrointestinal disorder (EGID).

What happened next?

The patient was advised to avoid wheat, eggs and cow's milk. He was started on Prevacid 30 mg po daily, prednisone syrup 1mg/ml, 5ml po daily for 4 weeks and advised to continue the iron syrup.

At follow-up, the patient's CBC showed Hb 12.3 mg/dL, Hct 38.9, eosinophils 2% (186). Steroids were tapered off and oral fluticasone was started. A follow-up EGD was scheduled in 6 months.

Summary

Primary eosinophilic gastrointestinal disorders are defined as disorders that selectively affect the gastrointestinal tract with eosinophil-rich inflammation in the absence of known causes for eosinophilia (eg, drug reactions, parasitic infections, and malignancy).

These disorders include eosinophilic esophagitis, eosinophilic gastritis, eosinophilic gastroenteritis, eosinophilic enteritis, and eosinophilic colitis and are occurring with increasing frequency.

References

Eosinophilic gastrointestinal disorders (EGID). Rothenberg ME. Eosinophilic gastrointestinal disorders (EGID).
Eosinophilic Gastroenteritis. eMedicine Specialties > Gastroenterology > Intestine. eMedicine, 2009.

Published: 12/07/2009
Updated: 09/07/2010

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