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  Table of Contents  
LETTER TO EDITOR
Year : 2022  |  Volume : 43  |  Issue : 2  |  Page : 220-221
 

A rare case of genital porokeratosis associated with epididymo-orchitis


1 Department of Dermatology, Jawaharlal Nehru Medical College, Aligarh Muslim University, Aligarh, Uttar Pradesh, India
2 Department of Pathology, Jawaharlal Nehru Medical College, Aligarh Muslim University, Aligarh, Uttar Pradesh, India

Date of Submission02-Jun-2022
Date of Decision29-Jun-2022
Date of Acceptance30-Jun-2022
Date of Web Publication17-Nov-2022

Correspondence Address:
Dr. Hania Qamar Khan
Department of Dermatology, Jawaharlal Nehru Medical College, Aligarh Muslim University, Aligarh, Uttar Pradesh
India
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Source of Support: None, Conflict of Interest: None


DOI: 10.4103/ijstd.ijstd_56_22

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How to cite this article:
Kulhari M, Khan HQ, Amin SS, Afrose R. A rare case of genital porokeratosis associated with epididymo-orchitis. Indian J Sex Transm Dis 2022;43:220-1

How to cite this URL:
Kulhari M, Khan HQ, Amin SS, Afrose R. A rare case of genital porokeratosis associated with epididymo-orchitis. Indian J Sex Transm Dis [serial online] 2022 [cited 2022 Nov 28];43:220-1. Available from: https://www.ijstd.org/text.asp?2022/43/2/220/361324


Sir,

Porokeratosis is a disorder of abnormal keratinization with varied clinical presentations in the form of localized and generalized disease.[1] Genital porokeratosis (GP) is a variant involving the scrotum, penis, buttocks, natal cleft, groins, and adjacent thighs. It is underreported as it mimics several venereal as well as nonvenereal dermatoses such as hypertrophic lichen planus, psoriasis, Bowen's disease, and dermatophytosis.[2] The exact etiology is yet unknown, but various trigger factors such as ultraviolet radiation, immunosuppression, drugs, malignancies, autoimmune diseases, and infections have been documented.[3] Here, we report a rare case of GP associated with bilateral acute on chronic epididymo-orchitis.

A 35-year-old immunocompetent male presented to the emergency department with fever and severe dragging scrotal pain for 3 days. No history of dysuria and burning or increased frequency of micturition was elicited. On further inquiry, he complained of dull aching pain in both testes and itchy lesions over the groin and scrotum for 1 year. Topical antifungal creams yielded no result. No other significant personal or family history was elicited.

On examination, multiple hyperpigmented papules and plaques with fine scaling and elevated peripheral rim, of size 1–3 cm in diameter, were visible discretely over the scrotum, bilateral inner thighs, and buttocks [Figure 1]a and [Figure 1]b. Both testes were enlarged and tender, associated with thickened spermatic cords. Dermoscopy of plaques showed a well-defined lesion with a pale center, peripheral track-like border, and follicular plugging [Figure 2].
Figure 1: (a) Multiple keratotic papules and plaques with elevated scaly border and depressed center over the scrotum, and inner thighs bilaterally with scrotal swelling. (b) Well-defined keratotic plaques with raised border and depressed center

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Figure 2: Hyperpigmented well-defined plaque with follicular plugging and double-marginated track-like border (DermLite DL4 ×10)

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Investigation revealed normal hemogram, proteinuria (1+), and hematuria (1+). The urine culture was sterile. Ultrasonography showed tortuous and thickened bilateral spermatic cord with increased echogenicity and bilateral hydrocele. Skin biopsy from the border of the plaque depicted coronoid lamellae and pigmentary incontinence [Figure 3]. Based on these findings, a diagnosis of GP with chronic bilateral epididymo-orchitis with acute exacerbation was made. The patient was given topical 5-fluorouracil local application in the morning and topical tretinoin cream 0.025% cream at night locally along with oral isotretinoin 20mg at night. He was also advised tight scrotal support with oral levofloxacin 750mg once a day from the surgery unit. The patient is on regular follow-up and partial subsidence of lesions is seen after 1 month of treatment.
Figure 3: Coronoid lamella with pigmentary incontinence in the papillary dermis. (H and E ×400)

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Chronic epididymo-orchitis is defined as scrotal pain lasting at least 3 months in duration and classified as inflammatory, obstructive, or epididymalgia.[4] Common infective causes include acute or preceding bacterial infections such as chlamydia and gonococcus in age <35 years, whereas coliforms and Pseudomonas are implicated in older males.[5] Our patient had features of chronic epididymitis, and acute exacerbation of pain with scrotal swelling suggesting acute epididymo-orchitis. The absence of urinary symptoms and sterile culture indicated that proteinuria and hematuria were secondary to epididymitis.

The infections found to be associated with porokeratosis are human immunodeficiency virus, herpes simplex, Streptococcus, hepatitis C, Leishmania, and human papillomavirus, but have been reported but in disseminated forms.[6] Chronic friction has been postulated to be a causative factor for GP, with no infectious agents demonstrated from the lesions. In a study, syphilis, condyloma acuminata, and folliculitis were associated in patients with GP.[7]

In our case, porokeratosis was present over the scrotum, buttocks, and adjacent thighs and was associated with acute on chronic bilateral epididymo-orchitis, which has not been reported in the literature. Acute epididymo-orchitis and porokeratosis are unrelated conditions, and GP was an incidental finding in our patient who presented with scrotal swelling and pain. Due to the simultaneous onset of lesions and chronic testicular pain, we suspect a common infectious etiology in both conditions, requiring further investigations such as polymerase chain reaction or nucleic acid amplification tests, which could not be done in our case due to logistic reasons. Thorough cutaneous and systemic examination and investigations in cases of GP should be done to establish if such association is definite or coincidental.

Declaration of patient consent

The authors certify that they have obtained all appropriate patient consent forms. In the form, the patient has given his consent for his images and other clinical information to be reported in the journal. The patient understands that name and initials will not be published and due efforts will be made to conceal his identity, but anonymity cannot be guaranteed.

Financial support and sponsorship

Nil.

Conflicts of interest

There are no conflicts of interest.



 
   References Top

1.
Das A, Vasudevan B, Talwar A. Porokeratosis: An enigma beginning to unravel. Indian J Dermatol Venereol Leprol 2022;88:291-9.  Back to cited text no. 1
    
2.
Joshi R, Minni K. Genitogluteal porokeratosis: A clinical review. Clin Cosmet Investig Dermatol 2018;11:219-29.  Back to cited text no. 2
    
3.
Laino L, Pala S, Innocenzi D, Accappaticcio G, Van Steensel MA. Genital porokeratosis. Eur J Dermatol 2004;14:190-2.  Back to cited text no. 3
    
4.
Nickel JC. Chronic epididymitis: A practical approach to understanding and managing a difficult urologic enigma. Rev Urol 2003;5:209-15.  Back to cited text no. 4
    
5.
Berger RE, Alexander ER, Harnisch JP, Paulsen CA, Monda GD, Ansell J, et al. Etiology, manifestations and therapy of acute epididymitis: Prospective study of 50 cases. J Urol 1979;121:750-4.  Back to cited text no. 5
    
6.
Vargas-Mora P, Morgado-Carrasco D, Fustà-Novell X. Porokeratosis: A review of its pathophysiology, clinical manifestations, diagnosis, and treatment. Actas Dermosifiliogr (Engl Ed) 2020;111:545-60.  Back to cited text no. 6
    
7.
Gu CY, Zhang CF, Chen LJ, Xiang LH, Zheng ZZ. Clinical analysis and etiology of porokeratosis. Exp Ther Med 2014;8:737-41.  Back to cited text no. 7
    


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  [Figure 1], [Figure 2], [Figure 3]



 

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