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Journal of Clinical and
Medical Images
Headache and Rash in a Healthy Adult Male
Elias Impens1
, Steven Bialick2
and John Stern3
1
Department of Internal Medicine, Pennsylvania Hospital, 800 Spruce Street, Philadelphia, PA19107, USA
2
Department of Internal Medicine, University of Pennsylvania, Philadelphia, PA, USA
ISSN: 2640-9615
Clinical Image
3
Pennsylvania Hospital, Penn Infectious Diseases & Travel Medicine, 301 S 8th Street, Suite 1B, Philadelphia, PA 19106, USA
1. Keywords:
Cryptococcosis; idiopathic CD4+ T-cell lymphocytopenia; Opportunistic Infections
2. Clinical Image
A 50-year-old male with a past medical history of psoriasis presented with a two-week history of
progressively worsening fatigue, low-grade fevers and throbbing frontal headaches, and several
ulcerated papules of varying size (1-5mm) with central crusting and surrounding erythema noted
on the forearms, chest, back and feet (Figure 1). A lumbar puncture (LP) demonstrated an elevated
opening pressure and detection of cryptococcal antigen in the cerebral spinal fluid (CSF). HIV-
screen was repeatedly negative. Magnetic resonance imaging (MRI) of the brain revealed cerebral
atrophy.
This case should raise suspicion for disseminated cryptococcosis. Its rash frequently presents as
molluscum contagiosum-like umbilicated papules of varying sizes, but many other manifestations
(including vegetating crusted plaques or ulcers) have also been visualized. Disseminated crypto-
coccosis is rare in the absence of acquired immunodeficiency syndrome (AIDS) or use of immuno-
suppressive agents, and usually suggests an underlying primary or secondary immunodeficiency
syndrome. Quantification of CD4+
lymphocyte count can reveal a rare but severe disorder called
idiopathic CD4+
T-cell lymphocytopenia (ICL). ICL is a rare disorder of the immune system, de-
fined by persistent CD4+
lymphopenia in the absence AIDS or any other cause of immunodefi-
ciency. It can present with severe opportunistic infections (OIs), most commonly disseminated
cryptococcosis, mycobacteria, candida, and varicella [1,2].
Interestingly, though overlap exists among OIs in ICL and AIDS patients, the OIs with the high-
est incidence in ICL patients are cryptococcal and mycobacterial compared to pneumocystis and
candidiasis in AIDS patients [2]. Although the etiology of ICL is unknown, proposed mechanisms
include CD4+
lymphocyte loss due to increased activation and turnover or accelerated CD4+
lym-
phocyte apoptosis [3]. The disease can remain clinically silent, but most commonly manifests in
adulthood upon acquiring an OI [4].
*Corresponding Author (s): Elias Impens, Department of Internal Medicine, Pennsyl-
vania Hospital, 800 Spruce Street, Philadelphia, PA19107, USA, E-mail:elias.impens@
pennmedicine.upenn.edu
Citation: Elias Impens, Headache and Rash in a Healthy Adult Male. Journal of Clinical and Medical Im-
ages. 2019; V2(5): 1-2.
clinandmedimages.com
Volume 2 Issue 5- 2019
Received Date: 08 Dec 2019
Accepted Date: 22 Dec 2019
Published Date: 24 Dec 2019
Volume 2 Issue5 -2019 Clinical Image
Figure1: Ulcerated 2mm papule withcentral crusting and surrounding ery-
thema on the patient’s forearm (arrow).
References
1. Gholamin M, Bazi A, Abbaszadegan MR. Idiopathic lymphocytope-
nia. CurrOpinHematol. 2015; 22(1):46-52.
2. Ahmad DS, Esmadi M, Steinmann WC. Idiopathic CD4 Lymphocyto-
penia: Spectrum of opportunistic infections, malignancies, and autoim-
mune diseases. Avicenna J Med. 2013; 3(2): 37-47.
3. Karin Nielsen-Saines M, MPH. Idiopathic CD4+ lymphocytopenia.
2019.
4. Idiopathic CD4 positive T-lymphocytopenia. Genetic and Rare Dis-
eases Information Center. 2019.
Copyright ©2019 Elias Impens al This is an open access article distributed under the terms of the Creative Commons Attribution License,
which permits unrestricted use, distribution, and build upon your work non-commercially. 2

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Headache and Rash in a Healthy Adult Male

  • 1. Journal of Clinical and Medical Images Headache and Rash in a Healthy Adult Male Elias Impens1 , Steven Bialick2 and John Stern3 1 Department of Internal Medicine, Pennsylvania Hospital, 800 Spruce Street, Philadelphia, PA19107, USA 2 Department of Internal Medicine, University of Pennsylvania, Philadelphia, PA, USA ISSN: 2640-9615 Clinical Image 3 Pennsylvania Hospital, Penn Infectious Diseases & Travel Medicine, 301 S 8th Street, Suite 1B, Philadelphia, PA 19106, USA 1. Keywords: Cryptococcosis; idiopathic CD4+ T-cell lymphocytopenia; Opportunistic Infections 2. Clinical Image A 50-year-old male with a past medical history of psoriasis presented with a two-week history of progressively worsening fatigue, low-grade fevers and throbbing frontal headaches, and several ulcerated papules of varying size (1-5mm) with central crusting and surrounding erythema noted on the forearms, chest, back and feet (Figure 1). A lumbar puncture (LP) demonstrated an elevated opening pressure and detection of cryptococcal antigen in the cerebral spinal fluid (CSF). HIV- screen was repeatedly negative. Magnetic resonance imaging (MRI) of the brain revealed cerebral atrophy. This case should raise suspicion for disseminated cryptococcosis. Its rash frequently presents as molluscum contagiosum-like umbilicated papules of varying sizes, but many other manifestations (including vegetating crusted plaques or ulcers) have also been visualized. Disseminated crypto- coccosis is rare in the absence of acquired immunodeficiency syndrome (AIDS) or use of immuno- suppressive agents, and usually suggests an underlying primary or secondary immunodeficiency syndrome. Quantification of CD4+ lymphocyte count can reveal a rare but severe disorder called idiopathic CD4+ T-cell lymphocytopenia (ICL). ICL is a rare disorder of the immune system, de- fined by persistent CD4+ lymphopenia in the absence AIDS or any other cause of immunodefi- ciency. It can present with severe opportunistic infections (OIs), most commonly disseminated cryptococcosis, mycobacteria, candida, and varicella [1,2]. Interestingly, though overlap exists among OIs in ICL and AIDS patients, the OIs with the high- est incidence in ICL patients are cryptococcal and mycobacterial compared to pneumocystis and candidiasis in AIDS patients [2]. Although the etiology of ICL is unknown, proposed mechanisms include CD4+ lymphocyte loss due to increased activation and turnover or accelerated CD4+ lym- phocyte apoptosis [3]. The disease can remain clinically silent, but most commonly manifests in adulthood upon acquiring an OI [4]. *Corresponding Author (s): Elias Impens, Department of Internal Medicine, Pennsyl- vania Hospital, 800 Spruce Street, Philadelphia, PA19107, USA, E-mail:elias.impens@ pennmedicine.upenn.edu Citation: Elias Impens, Headache and Rash in a Healthy Adult Male. Journal of Clinical and Medical Im- ages. 2019; V2(5): 1-2. clinandmedimages.com Volume 2 Issue 5- 2019 Received Date: 08 Dec 2019 Accepted Date: 22 Dec 2019 Published Date: 24 Dec 2019
  • 2. Volume 2 Issue5 -2019 Clinical Image Figure1: Ulcerated 2mm papule withcentral crusting and surrounding ery- thema on the patient’s forearm (arrow). References 1. Gholamin M, Bazi A, Abbaszadegan MR. Idiopathic lymphocytope- nia. CurrOpinHematol. 2015; 22(1):46-52. 2. Ahmad DS, Esmadi M, Steinmann WC. Idiopathic CD4 Lymphocyto- penia: Spectrum of opportunistic infections, malignancies, and autoim- mune diseases. Avicenna J Med. 2013; 3(2): 37-47. 3. Karin Nielsen-Saines M, MPH. Idiopathic CD4+ lymphocytopenia. 2019. 4. Idiopathic CD4 positive T-lymphocytopenia. Genetic and Rare Dis- eases Information Center. 2019. Copyright ©2019 Elias Impens al This is an open access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and build upon your work non-commercially. 2