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Review ArticlePractice

Numerous asymptomatic dermal cysts

Diagnosis and treatment of steatocystoma multiplex

Jorge R. Georgakopoulos, Arvin Ighani and Jensen Yeung
Canadian Family Physician December 2018; 64 (12) 892-899;
Jorge R. Georgakopoulos
Medical student in the Schulich School of Medicine and Dentistry at Western University in London, Ont.
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Arvin Ighani
Medical student at the University of Toronto in Ontario.
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Jensen Yeung
Lecturer and staff dermatologist in the Division of Dermatology at the University of Toronto.
MD FRCPC
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Abstract

Objective To provide family physicians with the information needed to recognize, diagnose, and discuss available treatment options for steatocystoma multiplex (SM).

Sources of information A comprehensive PubMed search using steatocystoma multiplex as either a text word or a MeSH term was conducted, and articles reporting on treatment outcomes were included.

Main message Steatocystoma multiplex is a benign disorder often characterized by numerous asymptomatic dermal cysts on the trunk, arms, axillae, face, thighs, and scalp. Psychological distress due to these undesirable lesions is not uncommon for this condition. A literature review identified the following SM treatments, all of which were associated with limitations: carbon dioxide laser, modified surgical techniques, cryotherapy, and medical management. Steatocystoma multiplex is challenging to treat and, at this time, effective management is most often achieved through patient education.

Conclusion Family physicians play a critical role in the early diagnosis and management of SM. Education about treatment options and managing patient expectations might greatly alleviate the psychosocial implications of this disease.

Steatocystoma multiplex (SM) is a benign disorder of the pilosebaceous unit, manifesting as multiple asymptomatic dermal cysts. Although sporadic presentation is most often reported, it is believed to have an autosomal dominant pattern of inheritance involving a keratin 17 mutation.1 The following described case and review of treatment options can be used as a learning tool for how to recognize, diagnose, and manage SM. Early disease recognition and patient education might play a critical role in alleviating psychological implications associated with this disease.

Case description

A 22-year-old woman presented to an academic dermatology clinic concerned about numerous bumps on her arms, thighs, and trunk. She was referred by her family doctor to confirm the diagnosis of SM and discuss treatment options for these cosmetically bothersome lesions. Physical examination revealed numerous yellow- to skin-coloured, firm, freely mobile papules and nodules on her arms, thighs, and trunk that had slowly enlarged and increased in number over 5 years (Figures 1A and 1B). Her family history was not relevant for similar lesions and no other cutaneous findings were identified at the time of presentation.

While her history and physical examination findings strongly suggested the diagnosis of SM, the patient requested a biopsy to obtain a definitive answer. Two punch biopsies were taken of subcutaneous nodules using a 4-mm full-thickness punch at 2 separate sites. Histopathology revealed encapsulated cysts lined by several layers of epithelial cells folded in an irregular manner. The cystic lumen was lined with a thick eosinophilic band. These findings confirmed the diagnosis of SM. The contents of the cyst could not be elucidated by the pathologist; however, vellus hairs and hair follicles are commonly observed under microscopy.2

Figure 1.
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Figure 1.

Steatocystoma multiplex: Numerous skin-coloured, firm papules and nodules on A) the back and B) the forearm of a female patient.

Sources of information

A review of the PubMed database was conducted and relevant studies were retrieved using steatocystoma multiplex as either a text word or a MeSH term on March 20, 2017. The initial search yielded 231 articles for screening (Figure 2). After abstract and full-text review, primary articles (ie, case reports or case series) reporting treatment outcomes for SM were identified for inclusion in this review of treatment options. In addition, manual reviews of citation lists for relevant articles were performed.

Figure 2.
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Figure 2.

Flowchart of study selection process: Review of treatment options for steatocystoma multiplex.

Main message

Common presentation.

Steatocystoma multiplex papules or nodules commonly present on areas with densely concentrated pilosebaceous units including the trunk, arms, axillae, face, thighs, scalp, and less commonly the genitals and breasts.3–6 It most frequently presents in adolescence or early adulthood, with a mean age of 26 years at the time of diagnosis, and has no predilection for sex.7 Although the lesions are asymptomatic, with no malignant potential, patients often seek treatment options owing to the psychological distress caused by the cosmetically undesirable lesions. The case described here represents the classic presentation of SM and highlights the important role family physicians can play in early disease recognition.

Diagnosis.

Although SM shares similar characteristics with other diseases, its diagnosis is often made through history and physical examination alone.8 Pathologic analysis of sebaceous cysts, such as those seen in SM, provides little value when there is a low index of concern for malignancy. For this reason, a diagnosis of SM based on clinical findings is often warranted unless clinical suspicion suggests otherwise.8 If a biopsy is required, multiple samples should be taken because variations in the classic histopathologic features of SM have been described.2 A 4-mm full-thickness punch biopsy is recommended.

Evaluation and differential diagnosis.

Despite the benign and often asymptomatic nature of this disease, an inflammatory variant known as steatocystoma multiplex suppurativa (SMS) can present.2 This is seen in a male patient who presented to the clinic with numerous SM lesions on his chest, some of which were inflamed (Figure 3). The inflamed lesions of SMS pose a great risk of infection, purulent discharge, and scarring.9 A mixed presentation of asymptomatic and inflamed lesions is common. Additionally, SM might mimic other common skin disorders, sometimes leading to misdiagnosis and unnecessary treatment. The clinical appearance of SM can resemble acne vulgaris, vellus cyst, epidermoid or dermoid cyst, hidradenitis suppurativa, milia, follicular infundibular tumours, and lipomas.10

Figure 3.
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Figure 3.

Steatocystoma multiplex suppurativa: Mixed presentation of steatocystoma multiplex with suppurativa inflammatory variant involvement on the chest of a male patient.

Treatment options.

Although SM is difficult to treat, having a strong understanding of all available treatment options, with a focus on recurrence and cosmetic outcomes, is crucial for patient education and disease perception. A total of 37 relevant publications describing treatment outcomes of SM patients were identified and are summarized in Table 1.3–5,9,11–43 Goals of SM treatment include substantial reduction of cyst size, prevention of recurrence, good cosmetic outcome, and patient satisfaction. At this time, no treatment can prevent the formation of new lesions. Positive outcomes are often challenging to achieve, as the described treatment methods are associated with limitations. Effective management is most often achieved through patient education. However, recent advanced techniques include the following.

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Table 1.

Summary of available publications describing treatment outcomes for SM, by treatment

Carbon dioxide laser: Carbon dioxide laser has recently been shown to successfully treat multiple lesions in a single session with good cosmetic outcomes. However, this procedure might not be suited for larger cysts and is not easily accessible to all patients.11,12 This laser method is comparable to excising the lesion, as the wavelength of the laser ablates skin tissue.

Modified needle aspiration: Needle aspiration with gentle extirpation of cystic contents has proven successful, with excellent cosmetic outcomes.5,13,14 Despite good results, this treatment requires a skilled operator and does not work well on very large (> 15 mm in diameter) or small (< 3 mm in diameter) cysts. Recurrence rates are extremely high for this treatment method.

Modified surgical techniques: Surgical techniques, including fine incision followed by cyst wall extraction with forceps, vein hooks, or curette, show excellent cosmetic results but are time-consuming and invasive.4,15–17

Cryotherapy: Cryotherapy allows for the treatment of multiple lesions in a single session; however, it is greatly limited owing to the cosmetic disfigurement it causes and its extremely low efficacy.9,18

Medical management: Medical management with oral isotretinoin is the preferred treatment for SMS and it provides great reduction in inflammation.9,19,20 However, results are often not seen for months and recurrence following discontinuation has been reported.21,22 Mixed variants of both SM and SMS might require combination therapy.9,18 Isotretinoin has no effect on noninflamed lesions.20 A short course (2 to 4 weeks) of oral tetracycline, topical clindamycin, or benzoyl peroxide wash (ie, antibiotics with anti-inflammatory properties) might be considered for management of noninfectious inflammatory lesions.21,36

Case resolution

Two weeks after the biopsies were taken, the patient was seen in the clinic for consultation regarding her confirmed diagnosis of SM. After educational guidance, she was aware that this condition posed no medical risk and that treatment was not required or recommended. Owing to the extensive number of lesions and evidence showing that effective treatment often leads to scarring, the patient elected to forgo therapy at this time. She was instructed to return for follow-up should any changes occur, including extensive growth, discoloration, or severe inflammation suggesting infection.

Conclusion

Owing to limited evidence for effective treatment methods, SM is a therapeutically challenging diagnosis. The ability to identify multiple asymptomatic dermal cysts and recognize the characteristic pattern of multiplication and progressive growth seen in SM can allow for early education about the benign nature of this disease. Furthermore, a concrete understanding of treatment options, including risks and benefits, can play a critical role in managing the psychosocial implications of SM. Patients should be informed that effective treatment options are time-consuming and often result in scarring, and recurrence is common. Unrealistic expectations and risks of unnecessary treatment should be discussed in depth with this patient population, as these individuals might desire unattainable outcomes.

Notes

Editor’s key points

  • ▸ Steatocystoma multiplex is a benign disorder that presents as papules or nodules on areas with densely concentrated pilosebaceous units including the trunk, arms, axillae, face, thighs, scalp, and less commonly the genitals and breasts. Although the lesions are asymptomatic, with no malignant potential, patients often seek treatment options owing to the psychological distress caused by the cosmetically undesirable lesions.

  • ▸ Despite the benign and often asymptomatic nature of this disease, an inflammatory variant known as steatocystoma multiplex suppurativa can present. The inflamed lesions of steatocystoma multiplex suppurativa pose a great risk of infection, purulent discharge, and scarring.

  • ▸ Patients should be informed that effective treatment options are time-consuming and can result in scarring, and recurrence is common. Unrealistic expectations and risks of unnecessary treatment should be discussed in depth with this patient population.

Footnotes

  • Contributors

    All authors contributed to the literature review and interpretation, and to preparing the manuscript for submission.

  • Competing interests

    None declared

  • This article is eligible for Mainpro+ certified Self-Learning credits. To earn credits, go to www.cfp.ca and click on the Mainpro+ link.

  • This article has been peer reviewed.

  • La traduction en français de cet article se trouve à www.cfp.ca dans la table des matières du numéro de décembre 2018 à la page e517.

  • Copyright© the College of Family Physicians of Canada

References

  1. 1.↵
    1. Covello SP,
    2. Smith FJ,
    3. Sillevis Smitt JH,
    4. Paller AS,
    5. Munro CS,
    6. Jonkman MF,
    7. et al
    . Keratin 17 mutations cause either steatocystoma multiplex or pachyonychia congenita type 2. Br J Dermatol 1998;139(3):475-80.
    OpenUrlCrossRefPubMed
  2. 2.↵
    1. Plewig G,
    2. Wolff HH,
    3. Braun-Falco O
    . Steatocystoma multiplex: anatomic reevaluation, electron microscopy, and autoradiography. Arch Dermatol Res 1982;272(3–4):363-80.
    OpenUrlCrossRefPubMed
  3. 3.↵
    1. Kamra HT,
    2. Gadgil PA,
    3. Ovhal AG,
    4. Narkhede RR
    . Steatocystoma multiplex—a rare genetic disorder: a case report and review of the literature. J Clin Diagn Res 2013;7(1):166-8. Epub 2013 Jan 1.
    OpenUrl
  4. 4.↵
    1. Choudhary S,
    2. Koley S,
    3. Salodkar A
    . A modified surgical technique for steatocystoma multiplex. J Cutan Aesthet Surg 2010;3(1):25-8.
    OpenUrlPubMed
  5. 5.↵
    1. Oertel YC,
    2. Scott DM
    . Cytologic-pathologic correlations: fine needle aspiration of three cases of steatocystoma multiplex. Ann Diagn Pathol 1998;2(5):318-20.
    OpenUrlPubMed
  6. 6.↵
    1. Senel E
    . Steatocystoma multiplex [Dermacase]. Can Fam Physician 2010;56:667, 672.
    OpenUrlFREE Full Text
  7. 7.↵
    1. Cho S,
    2. Chang SE,
    3. Choi JH,
    4. Sung KJ,
    5. Moon KC,
    6. Koh JK
    . Clinical and histologic features of 64 cases of steatocystoma multiplex. J Dermatol 2002;29(3):152-6.
    OpenUrlPubMed
  8. 8.↵
    1. Gargya V,
    2. Lucas HD,
    3. Wendel Spiczka AJ,
    4. Mahabir RC
    . Is routine pathologic evaluation of sebaceous cysts necessary?: a 15-year retrospective review of a single institution. Ann Plast Surg 2017;78(2):e1-3.
    OpenUrl
  9. 9.↵
    1. Apaydin R,
    2. Bilen N,
    3. Bayramgürler D,
    4. Başdaş F,
    5. Harova G,
    6. Dökmeci C
    . Steatocystoma multiplex suppurativum: oral isotretinoin treatment combined with cryotherapy. Australas J Dermatol 2000;41(2):98-100.
    OpenUrlPubMed
  10. 10.↵
    1. Vivas A,
    2. Keri J
    . Steatocystoma multiplex. In: Zeichner JA, editor. Acneiform eruptions in dermatology. A differential diagnosis. New York, NY: Springer; 2014. p. 343-8.
  11. 11.↵
    1. Kassira S,
    2. Korta DZ,
    3. de Feraudy S,
    4. Zachary CB
    . Fractionated ablative carbon dioxide laser treatment of steatocystoma multiplex. J Cosmet Laser Ther 2016;18(7):364-6. Epub 2016 Jul 19.
    OpenUrl
  12. 12.↵
    1. Bakkour W,
    2. Madan V
    . Carbon dioxide laser perforation and extirpation of steatocystoma multiplex. Dermatol Surg 2014;40(6):658-62.
    OpenUrl
  13. 13.↵
    1. Moody MN,
    2. Landau JM,
    3. Goldberg LH,
    4. Friedman PM
    . 1450-nm diode laser in combination with the 1550-nm fractionated erbium-doped fiber laser for the treatment of steatocystoma multiplex: a case report. Dermatol Surg 2012;38(7 Pt 1):1104-6. Epub 2012 Apr 9.
    OpenUrlPubMed
  14. 14.↵
    1. Varshney M,
    2. Aziz M,
    3. Maheshwari V,
    4. Alam K,
    5. Jain A,
    6. Arif SH,
    7. et al
    . Steatocystoma multiplex. BMJ Case Rep 2011;2011. bcr0420114165.
  15. 15.↵
    1. Mumcuoğlu CT,
    2. Gurel MS,
    3. Kiremitci U,
    4. Erdemir AVT,
    5. Karakoca Y,
    6. Huten O
    . Er:YAG laser therapy for steatocystoma multiplex. Indian J Dermatol 2010;55(3):300-1.
    OpenUrlPubMed
  16. 16.
    1. Madan V,
    2. August PJ
    . Perforation and extirpation of steatocystoma multiplex. Int J Dermatol 2009;48(3):329-30.
    OpenUrlCrossRefPubMed
  17. 17.↵
    1. Riedel C,
    2. Brinkmeier T,
    3. Kutzne H,
    4. Plewig G,
    5. Frosch PJ
    . Late onset of a facial variant of steatocystoma multiplex—calretinin as a specific marker of the follicular companion cell layer. J Dtsch Dermatol Ges 2008;6(6):480-2.
    OpenUrlPubMed
  18. 18.↵
    1. Rossi R,
    2. Cappugi P,
    3. Battini M,
    4. Mavilia L,
    5. Campolmi P
    . CO laser therapy in a case of steatocystoma multiplex with prominent nodules on the face and neck. Int J Dermatol 2003;42(4):302-4.
    OpenUrlCrossRefPubMed
  19. 19.↵
    1. Krähenbühl A,
    2. Eichmann A,
    3. Pfaltz M
    . CO2 laser therapy for steatocystoma multiplex. Dermatologica 1991;183(4):294-6.
    OpenUrlPubMed
  20. 20.↵
    1. Kumar S,
    2. Kurien NM,
    3. Menon V
    . Steatocystoma multiplex of face: a case report. Int J Case Rep Imag 2014;5(3):207-10.
    OpenUrl
  21. 21.↵
    1. Gordon Spratt EA,
    2. Kaplan J,
    3. Patel RR,
    4. Kamino H,
    5. Ramachandran SM
    . Steatocystoma. Dermatol Online J 2013;19(12):20721.
    OpenUrl
  22. 22.↵
    1. Lee SJ,
    2. Choe YS,
    3. Park BC,
    4. Lee WJ,
    5. Kim DW
    . The vein hook successfully used for eradication of steatocystoma multiplex. Dermatol Surg 2007;33(1):82-4.
    OpenUrlCrossRefPubMed
  23. 23.
    1. Ichikawa K,
    2. Akamatsu T,
    3. Tanino R,
    4. Miyasaka M
    . Surgical treatment of facial steatocystoma multiplex. Eur J Plast Surg 2006;29(2):81-4.
    OpenUrl
  24. 24.
    1. Düzova AN,
    2. Șentürk GB
    . Suggestion for the treatment of steatocystoma multiplex located exclusively on the face. Int J Dermatol 2004;43(1):60-2.
    OpenUrlPubMed
  25. 25.
    1. Kaya TI,
    2. Ikizoglu G,
    3. Kokturk A,
    4. Tursen U
    . A simple surgical technique for the treatment of steatocystoma multiplex. Int J Dermatol 2001;40(12):785-8.
    OpenUrlCrossRefPubMed
  26. 26.
    1. Schmook T,
    2. Burg G,
    3. Hafner J
    . Surgical pearl: mini-incisions for the extraction of steatocystoma multiplex. J Am Acad Dermatol 2001;44(6):1041-2.
    OpenUrlPubMed
  27. 27.
    1. Adams BB,
    2. Mutasim DF,
    3. Nordlund JJ
    . Steatocystoma multiplex: a quick removal technique. Cutis 1999;64(2):127-30.
    OpenUrl
  28. 28.
    1. Pamoukian VN,
    2. Westreich M
    . Five generations with steatocystoma multiplex congenita: a treatment regimen. Plast Reconstr Surg 1997;99(4):1142-6.
    OpenUrl
  29. 29.
    1. Kanekura T,
    2. Kawamura K,
    3. Nishi M,
    4. Kanzaki T
    . A case of steatocystoma multiplex with prominent cysts on the scalp treated successfully using a simple surgical technique. J Dermatol 1995;22(6):438-40.
    OpenUrlPubMed
  30. 30.
    1. Sato K,
    2. Shibuya K,
    3. Taguchi H,
    4. Kitano Y,
    5. Yoshikawa K
    . Aspiration therapy in steatocystoma multiplex. Arch Dermatol 1993;129(1):35-7.
    OpenUrlCrossRefPubMed
  31. 31.
    1. Keefe M,
    2. Leppard BJ,
    3. Royle G
    . Successful treatment of steatocystoma multiplex by simple surgery. Br J Dermatol 1992;127(1):41-4.
    OpenUrlPubMed
  32. 32.
    1. Feinstein A,
    2. Trau H,
    3. Movshovitz M,
    4. Schewach-Millet M
    . Steatocystoma multiplex. Cutis 1983;31(4):425-7.
    OpenUrl
  33. 33.
    1. Holmes R,
    2. Black MM
    . Steatocystoma multiplex with unusually prominent cysts on the face. Br J Dermatol 1980;102(6):711-3.
    OpenUrlCrossRefPubMed
  34. 34.
    1. Egbert BM,
    2. Price NM,
    3. Segal RJ
    . Steatocystoma multiplex. Report of a florid case and a review. Arch Dermatol 1979;115(3):334-5.
    OpenUrlCrossRefPubMed
  35. 35.
    1. Lima Santana CNL,
    2. do Nascimento Pereira D,
    3. Paixão Lisboa A,
    4. Martins Leal J,
    5. Lago Obadia D,
    6. Souto da Silva R
    . Steatocystoma multiplex suppurativa: case report of a rare condition. An Bras Dermatol 2016;91(5 Suppl 1):51-3.
    OpenUrl
  36. 36.↵
    1. Adams B,
    2. Shwayder T
    . Steatocystoma multiplex suppurativum. Int J Dermatol 2008;47(11):1155-6.
    OpenUrlCrossRefPubMed
  37. 37.
    1. Moritz DL,
    2. Silverman RA
    . Steatocystoma multiplex treated with isotretinoin: a delayed response. Cutis 1988;42(5):437-9.
    OpenUrl
  38. 38.
    1. Friedman SJ
    . Treatment of steatocystoma multiplex and pseudofolliculitis barbae with isotretinoin. Cutis 1987;39(6):506-7.
    OpenUrl
  39. 39.
    1. Rosen BL,
    2. Brodkin RH
    . Isotretinoin in the treatment of steatocystoma multiplex: a possible adverse reaction. Cutis 1986;37(2):115, 120.
    OpenUrl
  40. 40.
    1. Statham BN,
    2. Cunliffe WJ
    . The treatment of steatocystoma multiplex suppurativum with isotretinoin. Br J Dermatol 1984;111(2):246.
    OpenUrlCrossRefPubMed
  41. 41.
    1. Schwartz JL,
    2. Goldsmith LA
    . Steatocystoma multiplex suppurativum: treatment with isotretinoin. Cutis 1984;34(2):149-50, 153.
    OpenUrl
  42. 42.
    1. Fekete GL,
    2. Fekete JE
    . Steatocystoma multiplex generalisata partially suppurativa—case report. Acta Dermatovenerol Croat 2010;18(2):114-9.
    OpenUrl
  43. 43.↵
    1. Notowicz A
    . Treatment of lesions of steatocystoma multiplex and other epidermal cysts by cryosurgery. J Dermatol Surg Oncol 1980;6(2):98-9.
    OpenUrlPubMed
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Canadian Family Physician: 64 (12)
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Numerous asymptomatic dermal cysts
Jorge R. Georgakopoulos, Arvin Ighani, Jensen Yeung
Canadian Family Physician Dec 2018, 64 (12) 892-899;

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