Tinea Cruris

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Continuing Education Activity

Tinea cruris, also known as jock itch, is an infection involving the genital, pubic, perineal, and perianal skin caused by pathogenic fungi known as dermatophytes. The evaluation and treatment of tinea cruris are discussed in the activity. This activity reviews the role of the healthcare team in improving care for patients with this condition. The activity will also highlight evidence-based therapeutics and lifestyle modifications to avoid common mistakes and mistreatments associated with the management of dermatophyte infections.


  • Identify the etiology of tinea cruris.
  • Outline the evaluation of tinea cruris.
  • Review the treatment options available for tinea cruris.
  • Describe interprofessional team strategies to improve the management of patients affected by tinea cruris.


Tinea cruris, also known as jock itch, is an infection involving the genital, pubic, perineal, and perianal skin caused by pathogenic fungi known as dermatophytes.[1][2][3][4][5] These dermatophytes affect keratinized structures such as hair and the epidermis' stratum corneum resulting in a characteristic rash. Intertriginous areas are hospitable environments for fungus, with sweating, maceration, and alkaline pH being responsible for the groin's predilection for infection.[1][3][4][5]

While tinea infections are often classified by the location of the body affected, they are also organized according to the responsible organism's primary source and mode of transmission.[3] Geophilic, zoophilic, and anthropophilic fungi are found in and transmitted by soil, animals, and humans, respectively.[1][3][6][7] Autoinfection of dermatophytes is also possible and especially crucial in tinea cruris as foot-to-groin spread can occur.[1]


Tinea cruris is caused by dermatophytes belonging to three genera, Trichophyton, Epidermophyton, and Microsporum.[5] Trichophyton rubrum has been isolated most commonly and remains the most frequent cause of tinea cruris worldwide; however, most studies do recognize the increasing prevalence of Trichophyton mentagrophytes and other organisms in certain regions.[1][2][3][4][7] Several risk factors have been identified that predispose an individual to tinea cruris, including excessive perspiration, occlusive clothing, improper hygiene, diabetes mellitus, immunocompromise, and lower socioeconomic status.[1][2][3][6]

Athletes, especially those involved in contact sports, may be more likely to contract tinea infections.[1] Genetics can also make a patient more susceptible to dermatophytes.[3][6] Of all these factors, perspiration appears to be the most influential variable in the development of infection.[1][8] In India, an area affected disproportionately often with dermatophytes, a study was conducted in response to the increasing frequency of and decreased treatment efficacy for local tinea infections.[9] Diabetes mellitus, family members with tinea, and personal history of cooking food were found to be positively associated with chronic and relapsing disease.[9]


Cutaneous mycoses, including tinea cruris, affect 20 to 25 percent of the world's population.[3][10] Developing and tropical countries have an increased prevalence of dermatophyte infections secondary to high temperatures and increased humidity.[1][11] In the United States, there have been an estimated 29.4 million cases of superficial fungal infections and over 51 million reported physician visits.[6] Adolescent and adult males comprise the majority of patients seen for tinea cruris and are affected by the disorder with increased frequency.[1][2][11] Worldwide increases in the occurrence of dermatophytoses and the discovery of recalcitrant infections have caused global concern.[3][4][5][9]


A simplified explanation of the complex and not well-understood pathophysiology of dermatophytes includes the organism's use of proteinases to digest keratin found in the skin's stratum corneum.[6][12][7]


While not always necessary for diagnosis, a potassium hydroxide (KOH) preparation may reveal histology consistent with dermatophyte infections.[1][2][3] Characteristic findings include branching or non-branching septate hyphae and possible arthroconidiospores.[2][3]

History and Physical

Patients with tinea cruris present complaining of a pruritic rash involving the groin.[1][2] The area may be irritated and painful if maceration is present, and secondary infections may result in inflammation and discomfort.[2] Duration of symptoms, previous occurrences, similar rashes in other locations, and past treatments should be elucidated. Individuals should be questioned about any history of diabetes, immunocompromise, renal disease, or hepatic dysfunction.[13] Clinicians should inquire about excessive sweating, wardrobe changes, and personal hygiene habits. A review of the patient's environmental and occupation exposures, including people, pets, animals, and contaminated soil, may be contributory.[13]

On physical examination, an erythematous, scaly, annular plaque with a raised leading edge and central clearing can be visualized, extending anywhere from the groin, upper thigh, and perineum to the perianal region.[1][2]


In most cases, tinea cruris can be diagnosed clinically; however, several tests exist to investigate a rash of the groin with unknown etiology.[1][2][3] Potassium hydroxide (KOH) preparations, skin biopsy with periodic acid-Schiff (PAS) stain, and fungal cultures on Sabouraud’s agar media can be utilized when the diagnosis is in question or the case of recurrent or recalcitrant episodes.[1][2][3]

In general, the sample should be obtained from the leading edge of the lesion to ensure an adequate collection of infected scales.[1] Potassium hydroxide (KOH) mounts are generally procured with a scalpel scraping technique; however, new studies have indicated that utilizing a cellophane adhesive tape method may simplify the collection process, facilitate transportation, provide a higher quality sample, and improve slide preservation time.[14] 

Treatment / Management

Antifungals utilized in treating dermatophytoses, including tinea cruris, target the synthesis of ergosterol, a vital component of fungal plasma membranes.[4] Management strategies are similar worldwide; however, some countries have specific guidelines based on their region's fungal profile.[6] Topical therapies are effective and usually preferred.[2][4][6] Allylamines (terbinafine, butenafine, naftifine) and azoles (clotrimazole, miconazole, sulconazole, oxiconazole, econazole, ketoconazole) are the mainstays of topical treatment regimens. They are generally prescribed once or twice daily for two to four weeks.[1][3][6]

Deciding which agent to use should be based on patient compliance, cost, and medication accessibility, as there is insufficient data to directly compare the effectiveness of individual drugs and classes.[8][15][16][13] Allylamines have a potentially shorter treatment timeline, have demonstrated lower relapse rates, and their metabolism is independent of the cytochrome p450 system.[8][13] Azoles are not as costly as allylamines but often require a longer treatment duration.[8] One newer topical azole, luliconazole, requires only once daily application for one week and may improve patient compliance through a more convenient dosing schedule.[6] Ciclopirox olamine is an older topical preparation with a unique mechanism of action compared to the commonly used allylamines and azoles.[17] Recent studies have demonstrated a number of benefits to ciclopirox therapy; however, it remains an underutilized antifungal medication.[17]

Oral preparations exist to manage tinea cruris and are indicated for chronic, recurrent, and recalcitrant disease.[1][2][4][6] Extensive or diffuse rashes and patients with immunocompromise may also require systemic treatments.[4] Stratum corneum penetration and concentration maintenance, keratin adherence, patient tolerance, and a minimal drug interaction profile are hallmarks of the ideal systemic medication for dermatophytoses.[4] Oral terbinafine and itraconazole have favorable characteristics for dermatophyte management and are the most often prescribed.[4][15][16][13] Fluconazole has demonstrated efficacy in treating tinea cruris; however, it is not preferred due to its poor keratin adherence and prolonged treatment duration.[4] Griseofulvin has similar pharmacokinetic limitations as fluconazole, and it is more appropriately utilized in the management of tinea capitis than tinea cruris.[1][4][6] Due to its potential for hepatotoxicity, oral ketoconazole is no longer recommended for dermatophytoses.[1][2][4][15][16] Topical antifungal therapies may be used as an adjunct in patients requiring systemic treatment. Topical and oral antibiotics can be administered when a secondary bacterial infection is present.[3][13]

A commonly used alternative treatment known as Whitfield's ointment has insufficient evidence of benefit.[18] Nystatin, a frequently utilized treatment for cutaneous candida infections, is ineffective for managing dermatophytoses such as tinea cruris.[2] Combined topical corticosteroid and antifungal therapy remain controversial. Some studies have demonstrated improved cure rates with concomitant steroid and antifungal topical applications; however, these results were based on low-quality evidence.[18] While steroids may improve acute inflammation and itching, they may also fortify dermatophyte's plasma membranes rendering antifungal medications less effective.[4] Steroids also activate fungal metabolism and can potentially facilitate the worsening of the primary infection.[4] Tinea incognito is another possible complication of steroid administration where the typical presentation of tinea is masked, and diagnosis is delayed.[1] Currently, topical steroids are not recommended as part of an evidence-based tinea cruris treatment regimen.[2][3][2][18][13]

Differential Diagnosis

The differential diagnosis for tinea cruris includes several other dermatologic conditions affecting the groin with similar presentations. Candidiasis, erythrasma, psoriasis, and seborrheic dermatitis exhibit comparable signs and symptoms and are most commonly confused with the fungal groin infection. Unlike tinea cruris, candidal intertrigo frequently affects women, and the rash may involve the scrotum and penis in males.[1][2] Satellite lesions and erythema without central clearing are indicative of candida as opposed to tinea. The rash of erythrasma lacks an active border and demonstrates coral-red fluorescence on Wood lamp examination. Psoriasis will likely manifest in other areas in addition to the crural region. Seborrheic dermatitis presents with greasy scales on an erythematous base.[2]


Patients with tinea cruris who undergo an appropriate treatment course experience cure rates ranging from 80 to 90 percent.[19]


Failure of therapy and recurrence are the most likely complications of tinea cruris. They have been attributed to reinfection from close contacts, autoinfection from separate body locations, infection by uncommon species such as zoonoses, misdiagnosis, drug resistance, and non-adherence to the management plan.[3] Steroid use may suppress the physical signs of tinea cruris, making the diagnosis more difficult. Also, chronic application can result in skin atrophy and telangiectasias.[4] Secondary bacterial infection is another potential complication of tinea cruris.[3] Majocchi’s granuloma is an uncommon complication of cutaneous fungal infections in which dermatophytes disseminate into the subcutaneous tissue secondary to skin breakdown, immunosuppression, or topical steroid use resulting in a deep, inflammatory disease.[3][20] A dermatophytid reaction may result in an allergic response at a separate location from the original tinea site.[21]


Consultation with dermatology or infectious disease may be warranted in recurrent or recalcitrant cases.[3]

Deterrence and Patient Education

Patient education should focus on non-pharmacologic measures to treat and prevent recurrences of tinea cruris. Loose-fitting, non-restrictive garments should be encouraged, and clothing should not be donned until the underlying skin is completely dried.[3] Because autoinfection originating from tinea pedis may occur, patients should avoid walking barefoot, and protective footwear should be used in public facilities.[3][13] Identification and treatment of potentially infected contacts, whether human or animal, should be undertaken.[13] Self-treatment with over-the-counter antifungals and steroids should be discouraged as this may result in resistant or chronic infections and can hinder a clinician's ability to make an accurate and timely diagnosis.[4]

Enhancing Healthcare Team Outcomes

Tinea cruris is a prevalent pathology with a worldwide distribution and an extensive history of affecting human populations. Despite our familiarity with the condition, there has been limited research specific to this subset of dermatophyte infections. Renewed interest has emerged with the development of recalcitrant infections and concern over fungal resistance. Self-treatment with easy-to-access over-the-counter topical antifungal and steroid preparations have been implicated as a probable cause of the observed decrease in treatment efficacy. In the context of fungal resistance, newly developed formulations such as luliconazole and underutilized, older agents like ciclopirox may be beneficial. 

With regard to corticosteroids, there is conflicting data on the appropriateness of their use for tinea cruris. Current management principles and guidelines label them as mistreatment; however, continued investigations of their utility are underway. If a practitioner believes topical steroids may benefit a patient, close supervision should be maintained throughout the treatment course with continued consideration of known adverse event potential for the individual and public health outcomes. 

With an understanding of the changing landscape of this common condition, and by implementing an interprofessional healthcare team approach including primary care clinicians (including PAs and NPs), dermatologists, infectious disease specialists, pharmacists, and nursing, patient care and public health may be improved through targeted, conscientious mycological treatment, patient education, and antifungal stewardship. [Level 2] This interprofessional paradigm should lead to the best outcomes with minimal to no adverse events. [Level 5]

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Tinea Cruris
Tinea Cruris
Contributed by DermNetNZ
Article Details

Article Author

Micah M. Pippin

Article Author

Michael L. Madden

Article Editor:

Moushumi Das


5/29/2023 4:52:24 PM



Gupta AK, Chaudhry M, Elewski B. Tinea corporis, tinea cruris, tinea nigra, and piedra. Dermatologic clinics. 2003 Jul:21(3):395-400, v     [PubMed PMID: 12956194]


Ely JW, Rosenfeld S, Seabury Stone M. Diagnosis and management of tinea infections. American family physician. 2014 Nov 15:90(10):702-10     [PubMed PMID: 25403034]


Sahoo AK, Mahajan R. Management of tinea corporis, tinea cruris, and tinea pedis: A comprehensive review. Indian dermatology online journal. 2016 Mar-Apr:7(2):77-86. doi: 10.4103/2229-5178.178099. Epub     [PubMed PMID: 27057486]


Khurana A, Sardana K, Chowdhary A. Antifungal resistance in dermatophytes: Recent trends and therapeutic implications. Fungal genetics and biology : FG & B. 2019 Nov:132():103255. doi: 10.1016/j.fgb.2019.103255. Epub 2019 Jul 19     [PubMed PMID: 31330295]


Sardana K, Kaur R, Arora P, Goyal R, Ghunawat S. Is Antifungal Resistance a Cause for Treatment Failure in Dermatophytosis: A Study Focused on Tinea Corporis and Cruris from a Tertiary Centre? Indian dermatology online journal. 2018 Mar-Apr:9(2):90-95. doi: 10.4103/idoj.IDOJ_137_17. Epub     [PubMed PMID: 29644192]


Gupta AK, Foley KA, Versteeg SG. New Antifungal Agents and New Formulations Against Dermatophytes. Mycopathologia. 2017 Feb:182(1-2):127-141. doi: 10.1007/s11046-016-0045-0. Epub 2016 Aug 8     [PubMed PMID: 27502503]


Odom R. Pathophysiology of dermatophyte infections. Journal of the American Academy of Dermatology. 1993 May:28(5 Pt 1):S2-S7     [PubMed PMID: 8496407]


Nadalo D, Montoya C, Hunter-Smith D. What is the best way to treat tinea cruris? The Journal of family practice. 2006 Mar:55(3):256-8     [PubMed PMID: 16510062]


Singh S, Verma P, Chandra U, Tiwary NK. Risk factors for chronic and chronic-relapsing tinea corporis, tinea cruris and tinea faciei: Results of a case-control study. Indian journal of dermatology, venereology and leprology. 2019 Mar-Apr:85(2):197-200. doi: 10.4103/ijdvl.IJDVL_807_17. Epub     [PubMed PMID: 30719987]


Ameen M. Epidemiology of superficial fungal infections. Clinics in dermatology. 2010 Mar 4:28(2):197-201. doi: 10.1016/j.clindermatol.2009.12.005. Epub     [PubMed PMID: 20347663]


Vena GA, Chieco P, Posa F, Garofalo A, Bosco A, Cassano N. Epidemiology of dermatophytoses: retrospective analysis from 2005 to 2010 and comparison with previous data from 1975. The new microbiologica. 2012 Apr:35(2):207-13     [PubMed PMID: 22707134]


Samdani AJ. Dermatophyte growth and degradation of human stratum corneum in vitro (pathogenesis of dermatophytosis). Journal of Ayub Medical College, Abbottabad : JAMC. 2005 Oct-Dec:17(4):19-21     [PubMed PMID: 16599028]


Drake LA, Dinehart SM, Farmer ER, Goltz RW, Graham GF, Hardinsky MK, Lewis CW, Pariser DM, Skouge JW, Webster SB, Whitaker DC, Butler B, Lowery BJ, Elewski BE, Elgart ML, Jacobs PH, Lesher JL Jr, Scher RK. Guidelines of care for superficial mycotic infections of the skin: tinea corporis, tinea cruris, tinea faciei, tinea manuum, and tinea pedis. Guidelines/Outcomes Committee. American Academy of Dermatology. Journal of the American Academy of Dermatology. 1996 Feb:34(2 Pt 1):282-6     [PubMed PMID: 8642094]


Raghukumar S, Ravikumar BC. Potassium hydroxide mount with cellophane adhesive tape: a method for direct diagnosis of dermatophyte skin infections. Clinical and experimental dermatology. 2018 Dec:43(8):895-898. doi: 10.1111/ced.13573. Epub 2018 May 29     [PubMed PMID: 29845649]


Gupta AK, Cooper EA. Update in antifungal therapy of dermatophytosis. Mycopathologia. 2008 Nov-Dec:166(5-6):353-67. doi: 10.1007/s11046-008-9109-0. Epub 2008 May 14     [PubMed PMID: 18478357]


van Zuuren EJ, Fedorowicz Z, El-Gohary M. Evidence-based topical treatments for tinea cruris and tinea corporis: a summary of a Cochrane systematic review. The British journal of dermatology. 2015 Mar:172(3):616-41. doi: 10.1111/bjd.13441. Epub 2015 Feb 9     [PubMed PMID: 25294700]


Sonthalia S, Agrawal M, Sehgal VN. Topical Ciclopirox Olamine 1%: Revisiting a Unique Antifungal. Indian dermatology online journal. 2019 Jul-Aug:10(4):481-485. doi: 10.4103/idoj.IDOJ_29_19. Epub     [PubMed PMID: 31334080]


El-Gohary M, van Zuuren EJ, Fedorowicz Z, Burgess H, Doney L, Stuart B, Moore M, Little P. Topical antifungal treatments for tinea cruris and tinea corporis. The Cochrane database of systematic reviews. 2014 Aug 4:(8):CD009992. doi: 10.1002/14651858.CD009992.pub2. Epub 2014 Aug 4     [PubMed PMID: 25090020]


Hay R. Therapy of Skin, Hair and Nail Fungal Infections. Journal of fungi (Basel, Switzerland). 2018 Aug 20:4(3):. doi: 10.3390/jof4030099. Epub 2018 Aug 20     [PubMed PMID: 30127244]


Trocoli Drakensjö I, Vassilaki I, Bradley M. Majocchis Granuloma Caused by Trichophyton mentagrophytes in 2 Immunocompetent Patients. Actas dermo-sifiliograficas. 2017 Jan-Feb:108(1):e6-e8. doi: 10.1016/j.ad.2015.05.020. Epub 2016 Mar 4     [PubMed PMID: 26952202]


Mayser P. [Dermatophyte : Current situation]. Der Hautarzt; Zeitschrift fur Dermatologie, Venerologie, und verwandte Gebiete. 2017 Apr:68(4):316-323. doi: 10.1007/s00105-017-3933-4. Epub     [PubMed PMID: 28116455]