Georgina-Maria Sarika
Rony Shreberk-Hassidim
Alexander Maly2- 1Department of Dermatology
- 2Department of Pathology, Hadassah Medical Center, The Faculty of Medicine, Hebrew University of Jerusalem, Jerusalem, Israel
Acral necrotic ulcers in infancy are rare but have been described in type I interferonopathies. Herein, we present a case of an 8-year-old child who presented at the age of one month with severe ulceronecrotic lesions on the face and limbs with exacerbations following exposure to cold weather. Despite extensive investigation the case remains undiagnosed to this day. We hypothesize that this case represents a novel and yet unknown autoinflammatory disease.
Introduction
Cold induced pernio-like lesions with necrotic ulcers are rare in infancy and are usually associated with an underlying genetic autoinflammatory disease. Aicardi-Goutières syndrome (AGS), STING-associated vasculopathy with onset in infancy (SAVI), PLCG2-associated antibody deficiency and immune dysregulation (PLAID) and Proteasome-associated autoinflammatory syndromes (PRAAS); such as Nakajo-Nishimura syndrome (NNS) and Chronic Atypical Neutrophilic Dermatosis with Lipodystrophy (CANDLE), are some of the recognized cold-associated syndromes, that are characterized by acral ulceronecrotic lesions (Table 1). These autoinflammatory disorders are referred to as type I interferonopathies and are due to inborn errors in interferon (IFN) signaling, resulting in upregulation of IFNα (1–7). Patients suffering from these disorders tend to present early in life. Despite the distinct clinical phenotypes of each disorder in this group, clinical manifestations may overlap and are associated with high morbidity and mortality without treatment (8). Other conditions that might present with similar manifestations include prolidase deficiency, lupus erythematosus, systemic sclerosis, chilblains (pernio), cryoglobulinemia, cryofibrinogenemia and pyoderma gangranosum (9, 10).
Table 1. Characteristics of type I interferonopathies included in our differential diagnosis.
We report on an eight-year-old boy who has suffered since early infancy from cold-aggravated necrotic ulcers on the face and extremities. Despite extensive work-up, none of the aforementioned disorders have been confirmed and the case still remains undiagnosed.
Case presentation
The patient is an eight-year-old male born to non-consanguineous parents of Arab origin. He has three healthy siblings, and his pregnancy and delivery were normal. In January 2014, at the age of 5 months he presented to the Emergency Department of our hospital with acrofacial ulceronecrotic plaques which appeared initially at the age of 1 month over the cheeks and nose with subsequent development of similar lesions over the hands and feet. The parents reported exacerbations upon exposure to cold temperatures. At his arrival, he was hemodynamically stable and alert with no fever.
Physical examination on admission showed erythematous violaceous indurated plaques with central necrotic ulceration located over the tip of the nose, bilateral cheeks and ear helices. Similar lesions were seen on the knees and extensor surfaces of the arms (Figures 1A–C). There were no cardiopulmonary, gastrointestinal, genitourinary or ophthalmological abnormalities.
Figure 1. (A–C) Clinical features on admission at age 5-months: erythematous plaques with central necrosis on the tip of the nose and the cheeks bilaterally (A). Ulceration on the helix of the left ear (B) Right knee with erythematous plaques with yellow-brown central crusts (C).
The patient was admitted for further investigation and treatment. During his hospitalization he showed signs of poor feeding, weight loss and failure to thrive. A nasogastric tube was inserted that facilitated his feeding, improving his weight. Despite topical wound care and systemic antibiotics including cephalosporins and vancomycin, systemic corticosteroids and antifungals, no improvement was observed, with new lesions appearing on the right hand and right elbow after exposure to cold. In addition, the patient developed unexplained febrile episodes with concurrent deterioration of the ulcers. Extensive laboratory workup was performed, as follows: skin and blood cultures showed no evidence of microbial growth (bacteria, mycobacteria and fungi). Cutaneous leishmaniasis was also excluded by smear and polymerase chain reaction. Blood work showed normal kidney and liver function tests moderate leukocytosis and thrombocytosis, normal hemoglobin level and no marked elevation of C-reactive protein or erythrocyte sedimentation rate. Anti-nuclear antibodies, rheumatoid factor, anti-Ro, anti-La, immunoglobulins, cryoglobulins and cryofibrinogens, C3, C4, C-ANCA and P-ANCA were all within normal limit. A biochemical assay for prolidase deficiency was negative, chest x-ray, abdominal ultrasound, were normal. Serology for human immunodeficiency virus was negative as well.
Two skin biopsies were performed, demonstrating epidermal necrosis, mild parakeratosis, mild focal vacuolar degeneration and apoptosis of basal cell keratinocytes., mononuclear lymphohistiocytic infiltrate surrounding blood vessels, eccrine glands and hair follicles together with fat necrosis and hyalinization suggestive of lipodystrophy. No thickening of the basement membrane was observed (Figures 2A,B).
Figure 2. (A,B) Histopathological findings of skin biopsies: epidermal necrosis, a mononuclear perivascular and periadenxal infiltrate, fat necrosis with hyalinization. Changes compatible with lipodystrophy in the dermis and subcutaneous tissue. (Figure A: H&E, ×50, Figure B: H&E, ×100).
Given the history of transient sterile pyrexias with pernio-like skin lesions, ulcerations and lipodystrophy, a disorder of type I interferonopathy was suspected. Trio exome sequencing obtained from peripheral blood of the patient and his parents was negative for mutations in genes responsible for different type-1 interferonopathies that were included in our differential diagnosis. Mutations in candidate genes which may explain the phenotype of our patient were not identified as well.
Following prolonged admission and inconclusive investigations, the patient's diagnosis remained unclear. Severe scarring and deformity became noticeable with time. The patient was eventually transferred to a hospital in his hometown to continue follow up and rehabilitation. He returned for follow-up for the first time after his discharge in November 2021, 7 years later at the age of 8-years-old. Then, physical examination showed numerous dyspigmented atrophic scars on the face and ulcers covered with crusts and thick yellow scales on the extremities. Saddle nose, muscle wasting, lipodystrophy and joint contractures were noted. Sadly, on his recent follow up in our clinic in November 2022 he presented a similar but more strikingly debilitating picture (Figures 3A–C). There was no involvement of the trunk or the genital area. During winter months the patient continues to suffer from febrile episodes with worsening of his skin lesions.
Figure 3. (A–C) Clinical features on his last follow up at the age of 9-years. Dyspigmented atrophic plaques on the cheeks, nose, chin and lateral upper eyelidswith deformity and scarring. Dystrophic and wasted saddle nose (A). Right hand showing ulcerated plaques covered with thick crust and scale, dyspigmented atrophic scars and contractures of fingers (B). Muscle wasting and dyspigmented atrophic scars on the lower limbs, ulcerated plaques and swelling of the knees (C).
Discussion
We present here a rare and severe case of perniosis associated with lipodystrophy appearing in early infancy and associated with failure to thrive and arthropathy. Thorough laboratory and genetic investigations failed to reveal the cause for his severely disabling condition, although a mutation in a yet unknown gene is most likely. Unfortunately, insurance-related issues prevented us from performing genome sequencing to conclude his genetic workup.
Our primary differential diagnoses included the spectrum of type I interferonopathies, characterized by dysregulation of IFNα signaling leading to constitutive upregulation or downregulation of negative regulatory mechanisms of this pathway. These disorders tend to manifest with skin vasculopathy, chilblains and panniculitis/lipodystrophy, central nervous system disorders and interstitial lung disease. These features represent the “clinical IFN signature” (11); at least partially, our patient seems to share this clinical signature. Various methods were proposed in 2019 by Lamot et al., for type 1 interferon detection, however, none of these methods were available to perform in our clinical setting due to lack of medical insurance (12).
Type 1 interferonopathies are usually resistant to conventional treatments. However, two recent studies on the treatment of type-1 interferonopathies, including AGS and familial chilblain lupus, SAVI, NNS and CANDLE syndrome with Janus kinase (JAK) inhibitors, showed promising results with improvement of dermatological and systemic symptoms. There were no severe side effects reported, making it a safe treatment option in these difficult-to-treat and debilitating disorders (And while our patient's undiagnosed disease progresses into a chronic disability, we acknowledge the clinical similarities of his symptoms to those of the type I interferonopathies and consider if future empirical treatment with a JAK inhibitor is justified (13, 14).
To conclude, we presented a patient with early onset acral ulceronecrotic lesions associated with lipodystrophy. Unfortunately, despite our efforts, the patient currently remains undiagnosed and untreated. We hope that the publication of this unique case will enable others to identify similar cases and assist in solving this diagnostic and therapeutic challenge.
Data availability statement
The raw data supporting the conclusions of this article will be made available by the authors, without undue reservation.
Ethics statement
Written informed consent was obtained from the minor(s)' legal guardian/next of kin for the publication of any potentially identifiable images or data included in this article.
Author contributions
All authors contributed equally. All authors contributed to the article and approved the submitted version.
Acknowledgments
We would like to thank the patient and his family for their cooperation and consent for the inclusion of the details and pictures presented in this article.
Conflict of interest
The authors declare that the research was conducted in the absence of any commercial or financial relationships that could be construed as a potential conflict of interest.
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References
1. Livingston JH, Crow YJ. Neurologic phenotypes associated with mutations in TREX1, RNASEH2A, RNASEH2B, RNASEH2C, SAMHD1, ADAR1, and IFIH1: aicardi-goutières syndrome and beyond. Neuropediatrics. (2016) 47:355–60. doi: 10.1055/s-0036-1592307
2. Crow YJ, Manel N. Aicardi-Goutières syndrome and the type I interferonopathies. Nat Rev Immunol. (2015) 15:429–40. doi: 10.1038/nri3850
3. Wang Y, Wang F, Zhang X. STING-associated vasculopathy with onset in infancy: a familial case series report and literature review. Ann Transl Med. (2021) 9:176. doi: 10.21037/atm-20-6198
4. Aderibigbe OM, Priel DL, Lee CC, Ombrello MJ, Prajapati VH, Liang MG, et al. Distinct cutaneous manifestations and cold-induced leukocyte activation associated with PLCG2 mutations. JAMA Dermatol. (2015) 151:627–34. doi: 10.1001/jamadermatol.2014.5641
5. Kanazawa N. Nakajo-Nishimura syndrome: an autoinflammatory disorder showing pernio-like rashes and progressive partial lipodystrophy. Allergol Int. (2012) 61:197–206. doi: 10.2332/allergolint.11-RAI-0416
6. Torrelo A. CANDLE Syndrome as a paradigm of proteasome-related autoinflammation. Front Immunol. (2017) 8:927. doi: 10.3389/fimmu.2017.00927
7. McDermott A, Jacks J, Kessler M, Emanuel PD, Gao L. Proteasome-associated autoinflammatory syndromes: advances in pathogeneses, clinical presentations, diagnosis, and management. Int J Dermatol. (2015) 54:121–9. doi: 10.1111/ijd.12695
8. Gedik KC, Lamot L, Romano M, Demirkaya E, Piskin D, Torreggianiet S, et al. The 2021 European alliance of associations for rheumatology/American college of rheumatology points to consider for diagnosis and management of autoinflammatory type I interferonopathies: cANDLE/PRAAS, SAVI and AGS. Ann Rheum Dis. (2022) 81(5):601–13. doi: 10.1136/annrheumdis-2021-221814
9. Nyssen A, Benhadou F, Magnée M, André J, Koopmansch C, Wautrecht JC. Chilblains. Vasa. (2020) 49:133–40. doi: 10.1024/0301-1526/a000838
10. Maronese CA, Pimentel MA, Li MM, Genovese G, Ortega-Loayza AG, Marzano AV. Pyoderma Gangrenosum: an updated literature review on established and emerging pharmacological treatments. Am J Clin Dermatol. (2022) 23:615–34. doi: 10.1007/s40257-022-00699-8
11. d'Angelo DM, Di Filippo P, Breda L, Chiarelli F. Type I interferonopathies in children: an overview. Front Pediatr. (2021) 9:631329. doi: 10.3389/fped.2021.631329
12. Lamot L, Niemietz I, Brown KL. Methods for type I interferon detection and their relevance for clinical utility and improved understanding of rheumatic diseases. Clin Exp Rheumatol. (2019) 37:1077–83.30943143
13. Sanchez GAM, Reinhardt A, Ramsey S, Wittkowski H, Hashkes PJ, Berkun Y, et al. JAK1/2 Inhibition with baricitinib in the treatment of autoinflammatory interferonopathies. J Clin Invest. (2018) 128:3041–52. doi: 10.1172/JCI98814
Keywords: acrofacial necrotic ulcers, perniosis, lipodystrophy, type 1 interferonopathies, undiagnosed cases
Citation: Sarika G, Shreberk-Hassidim R, Maly A and Molho-Pessach V (2022) Acrofacial necrotic ulcers in an infant: An undiagnosed presentation. Front. Pediatr. 10:1069242. doi: 10.3389/fped.2022.1069242
Received: 13 October 2022; Accepted: 5 December 2022;
Published: 22 December 2022.
Edited by:
Shanmuganathan Chandrakasan, Emory University, United StatesReviewed by:
Lovro Lamot, University of Zagreb, CroatiaAngelo Valerio Marzano, University of Milan, Italy
© 2022 Sarika, Shreberk-Hassidim, Maly and Molho-Pessach. This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.
*Correspondence: Vered Molho-Pessach rverem@hadassah.org.il
Specialty Section: This article was submitted to Pediatric Immunology, a section of the journal Frontiers in Pediatrics