Keywords
case report; COVID-19; gland penile necrosis; leprosy; SARS-CoV-2
This article is included in the Emerging Diseases and Outbreaks gateway.
case report; COVID-19; gland penile necrosis; leprosy; SARS-CoV-2
In this version we only add information on hemostasis laboratory parameters after LMWH administration.
See the authors' detailed response to the review by Serena Bianchi and Diana Torge
See the authors' detailed response to the review by Harrina Erlianti Rahardjo
At the beginning of 2020, the World Health Organization declared novel coronavirus disease-2019 (COVID-19) infection as a pandemic which caused by severe acute respiratory syndrome coronavirus (SARS-CoV-2) that has led to a global health crisis due to acute respiratory distress syndrome (ARDS).1 Most cases have mild-to-moderate symptoms, with approximately 15% developing severe pneumonia, while about 5% developing ARDS and organ failure.2 Other serious complications related to SARS-CoV-19 infection include hypercoagulability and thrombotic vasculopathy with clinical manifestations such as coronary syndrome, deep vein thrombosis, ischemic stroke, and pulmonary embolism.3,4 Recently, other serious clinical manifestations associated with genitalia condition were reported in patients with SARS-CoV-2 infection with penile ischemia.5 In patients infected by SARS-CoV-2, penile priapism has also been reported.6,7 Some authors have speculated that these conditions related to COVID-19 may be due to severe hypercoagulability and thrombotic tendency observed in patients with COVID-19.5,8
On the other hand, penile involvement in leprosy is uncommon.9 Leprosy (also known as Hansen’s disease) is an infection caused by Mycobacterium leprae (M. leprae) that can damage the peripheral nerves and bone absorption. Leprosy has two distinct phases: direct infection of macrophages and Schwann cells and reactional episodes. Approximately 50% of patients with leprosy are affected by a reactional episode,10 which occurs because of endothelial inflammation leading to necrotizing pan-vasculitis. This condition, in severe cases, progresses to necrotic hemorrhagic lesions of the extremities and trunk, as well as Lucio’s phenomenon.11,12
Penile ischemia or necrosis is rare due to its abundant blood circulations. Usually, penile necrosis is associated with thrombotic phenomena and calcium deposits in patients on dialysis.13 However, no previous cases of penile ischemia in a COVID-19 patient who concomitantly infected with leprosy have ever been reported. Here, we presented a unique case of penile necrosis in acute COVID-19 and leprosy infection following the CARE guidelines.14 To the best of our knowledge, this case is the first case presenting penile glans necrosis in COVID-19 patient concomitant leprosy. We also described the potential pathophysiology of glans penis necrosis in this case through a literature review.
A 56-year-old Indonesian male patient was admitted to Dr. Zainoel Abidin General Hospital in Aceh, Indonesia. He was referred from a regional hospital with SARS-CoV-2 infection and necrotic penile glans. Complaints of changes in the color of the glans penis occur progressively without any past intervention. In addition, he also complained of pain in the penis, dysuria and difficulty urinating. He worked as a farmer, actively smoked since he was an adolescent, and does not consume any drugs or alcohol. Currently, he is undergoing treatment for leprosy disease. Table 1 summarizes the patient’s characteristics.
The patient has been diagnosed with leprosy since April 2021, he complained of a rash and atrophy of the hand muscles. Then the patient received leprosy treatment with a regiment of clofazimine 50 mg and Dapsone 100 mg.
This patient had a past medical history of hypertension, which is well-controlled with 10 mg/day oral amlodipine. There was no complaint in micturition, meatal discharge, and other genital problems.
On examination, his condition was stable with blood pressure 134/91 mmHg, pulse 90 bpm, respiratory 22 breaths/minute, and oxygen saturation at 97% on room temperature. The patient was afebrile and fully alert. His localized status found a discoloration involving the penile glans (Figure A).
An urgent radiologic investigation with Doppler ultrasound of the penile and pelvic computerized tomography (CT) angiography revealed no occlusion nor thrombus on the arteria that supplies the penile (Figure B).
The patient was admitted to the COVID ward with therapy as follows; 2 L/min nasal oxygen, 1000 mg ceftriaxone injection twice daily, 10 mg amlodipine daily, 50mg clofazimine daily, 100mg dapsone daily, 5000 U vitamin D daily, 1000 mg vitamin C daily and 300 international unit low molecular weight heparin (LMWH) intravenous drip daily for 4 days. No challenges were found during treatment.
After 4 days of LMWH administration without any treatment changes, the clinical condition of the gland penile and laboratory of hemostatic was improved, the necrosis was less extensive and limited to one-third of the superficial of the glans penis (Figure C). The patient then continued to isolate in the COVID-19 ward. On 6 weeks follow-up, the clinical and functional condition of the penis were excellent without any unexpected events. The patient’s urinary and erectile functions remained unchanged. The patient was also satisfied with the treatment that he received.
We searched four online databases (the Medline EMBASE, Google Scholar, PubMed, and Scopus) for the literature review. Four terms related to the patient’s condition were combined in the searching strategy; 1) Penile; 2) Penis; 3) COVID-19 and 4) SARS-CoV-2 to investigate the relationship between COVID-19 and leprosy infection in necrosis of glans penis. In the end, we found only one publication by Sarkis et al. that presented the penile ischemic condition in COVID-19 infection.5 This publication reported glans penile discoloration due to ischemia secondary to COVID-19. However, the patient had several comorbidities such as type 2 diabetes, hypertension, and end-stage kidney disease which could also be risk factors for thrombus vasculopathy.
Penile necrosis is linked to thrombotic events and calcium deposits in dialysis patients.13 Another study also reported penile necrosis secondary to purpura fulminans.15 One study in Japan described fifteen patients with penile necrosis due to calciphylaxis and a long history of diabetes.16 In this condition, it is clearly understood that diabetic vasculopathy and calcium deposits can become a thrombus which causes impaired blood flow to penis. In our patient, he had no comorbid precipitating thrombus vasculopathy. Although the patient is an active smoker, we still cannot conclude that this is the cause of penile necrosis. Uniquely, the CT angiography investigation of our patient did not reveal any occlusion or thrombus.
On the basis of the above finding, we hypothesized that the patient’s penis glans necrosis is caused by COVID-19 and leprosy co-infection. Many studies have published the role of microvascular thrombus in SARS-CoV-2 infection.17–20 There is a definite link between inflammation, hypercoagulation, and thrombosis, according to previous research. Part of this interaction is likely mediated by a cytokine storm, which increases the risk of developing disseminated intravascular coagulopathy.21 The stimulation of coagulation pathways throughout the body by mediators produced during a cytokine storm can result in a prothrombotic condition marked by the formation of microthrombi, diffuse capillary blockage, tissue ischemia, and organ damage.18 This pathogenesis indicates the possible tendency for physiopathology of glans penile necrosis secondary to SARS-CoV-2 infection.
Similar to SARS-CoV-2 infection, leprosy has long been known to trigger hemostasis disorders due to platelet abnormalities, blood coagulation, and fibrinolysis.10 Several studies have previously reported that patients with tuberculoid leprosy who develop erythema nodosum leprosum (ENL) had a longer activated partial thromboplastin time (aPTT) with elevated fibrinogen and platelet activation.12,22,23 One review of related studies conducted by Nery has described thrombophlebitis and pulmonary embolism in leprosy patients who develop ENL.24 Another study also found that leprosy disease was associated with coronary thrombosis and cerebral vascular accidents.25,26 These findings indicate that the severity of leprosy potentially leads to occlusion of blood flow which eventually causes organ damage.
We assume that patients co-infected with SARS-CoV-2 and leprosy have a greater risk of complications, especially hemostasis disorders and thrombus vasculopathy, as in our patient who showed elevated of D-Dimer and fibrinogen levels. This case report and literature review provide preliminary evidence of the association between SARS-CoV-2 and leprosy infection in glans penile necrosis; however, further studies are warranted.
This case report and literature review is limited by its short-term follow-up period, however its strength is that as we directly observed the patient rather than taking his information retrospectively, this reduces any potential bias.
Finally, several highlights should be considered in managing glans penile necrosis in patients with COVID-19 infection. As previously described, penile necrosis can occur as a result of a vasculopathy thrombus. On the other hand, COVID-19 and leprosy infection can also induce coagulopathy and microvascular thrombus. Therefore, choosing anticoagulant therapy than immediate aggressive amputation of the organ is still a viable option. Administering anti-thrombus therapy is a less-intrusive treatment approach that physicians can consider, which gave a good result in our patient.
In our perspective, microthrombus formation, diffuse capillary occlusion and tissue necrosis are the basis of the etiology penile glans necrosis in our patient. It is likely associated with SARS-CoV-2 and leprosy co-infection. This hypothesis makes this case an interesting report. In addition, from what we know at the time of writing this manuscript, this is the first case report of glans penile necrosis in a patient with SARS-CoV-2 and leprosy co-infection.
All data underlying the results are available as part of the article and no additional source data are required.
Written informed consent was obtained from the patient for publication of the patient’s images and this case report.
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Is the background of the case’s history and progression described in sufficient detail?
Partly
Are enough details provided of any physical examination and diagnostic tests, treatment given and outcomes?
Yes
Is sufficient discussion included of the importance of the findings and their relevance to future understanding of disease processes, diagnosis or treatment?
Yes
Is the case presented with sufficient detail to be useful for other practitioners?
Partly
References
1. Umakanthan S, Sahu P, Ranade AV, Bukelo MM, et al.: Origin, transmission, diagnosis and management of coronavirus disease 2019 (COVID-19).Postgrad Med J. 2020; 96 (1142): 753-758 PubMed Abstract | Publisher Full TextCompeting Interests: No competing interests were disclosed.
Reviewer Expertise: Microscopy, Anatomy, Morphology, Histology, Pathology
Competing Interests: No competing interests were disclosed.
Reviewer Expertise: Urology, functional urology, neurourology, urodynamic
Competing Interests: No competing interests were disclosed.
Reviewer Expertise: Urology, functional urology, neurourology, urodynamic
Is the background of the case’s history and progression described in sufficient detail?
Yes
Are enough details provided of any physical examination and diagnostic tests, treatment given and outcomes?
Partly
Is sufficient discussion included of the importance of the findings and their relevance to future understanding of disease processes, diagnosis or treatment?
Partly
Is the case presented with sufficient detail to be useful for other practitioners?
Partly
Competing Interests: No competing interests were disclosed.
Reviewer Expertise: Urology, functional urology, neurourology, urodynamic
Alongside their report, reviewers assign a status to the article:
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Version 2 (revision) 15 Mar 22 |
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Version 1 03 Feb 22 |
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