Case Reports in Dermatological Medicine http://www.hindawi.com The latest articles from Hindawi Publishing Corporation © 2016 , Hindawi Publishing Corporation . All rights reserved. A 27-Year-Old Severely Immunosuppressed Female with Misleading Clinical Features of Disseminated Cutaneous Sporotrichosis Mon, 04 Jan 2016 09:06:50 +0000 http://www.hindawi.com/journals/cridm/2016/9403690/ Sporotrichosis is a subacute or chronic granulomatous mycosis caused by fungus of the Sporothrix schenckii complex. It is considered to be a rare condition in most parts of the world. It mostly causes cutaneous infection but can also cause multisystemic disease. Unlike most deep cutaneous mycoses which have a primary pulmonary focus, it is usually caused by direct inoculation of the fungus into the skin causing a classical linear, lymphocutaneous nodular eruption. However, atypical presentations of the condition can occur especially in immunosuppressed individuals. We report the case of a severely immunosuppressed female who presented with disseminated cutaneous sporotrichosis which was initially diagnosed and treated as disseminated cutaneous Kaposi’s sarcoma. Atiyah Patel, Victor Mudenda, Shabir Lakhi, and Owen Ngalamika Copyright © 2016 Atiyah Patel et al. All rights reserved. Idiopathic Thrombocytopenic Purpura Misdiagnosed as Hereditary Angioedema Thu, 24 Dec 2015 12:36:17 +0000 http://www.hindawi.com/journals/cridm/2015/934247/ Hereditary angioedema is a rare, but potentially life-threatening genetic disorder that results from an autosomal dominant trait. It is characterized by acute, recurrent attacks of severe local edema, most commonly affecting the skin and mucosa. Swelling in hereditary angioedema patients does however not always have to be caused by angioedema but can relate to other concomitant disorders. In this report we are focusing on misdiagnosis in a patient with known hereditary angioedema, whose bleeding episode caused by idiopathic thrombocytopenic purpura was mistaken for an acute attack of hereditary angioedema. The case illustrates how clinicians can have difficulties in handling patients with rare diseases, especially in the emergency care setting. Michelle Fog Andersen and Anette Bygum Copyright © 2015 Michelle Fog Andersen and Anette Bygum. All rights reserved. Recurrent Thrombotic Vasculopathy in a Former Cocaine User Thu, 17 Dec 2015 11:34:02 +0000 http://www.hindawi.com/journals/cridm/2015/763613/ We report a case of a 35-year-old female who presented to the emergency room (ER) complaining of a pruritic rash involving multiple areas of the body. She had a significant history of cocaine use in the past. She had first developed a similar rash in 2013 when she was diagnosed with cocaine-induced vasculitis. Her urine toxicology had been positive for cocaine in the past until July 2013. She was incarcerated and attended a drug rehabilitation program after which she quit cocaine use, which was consistent with negative urine toxicology on subsequent admissions. Further workup did not reveal any other, autoimmune or infectious, etiology of this clinical presentation. The patient underwent biopsy of the skin lesion that was consistent with thrombotic vasculopathy likely secondary to levamisole. Preeti Jadhav, Hassan Tariq, Masooma Niazi, and Giovanni Franchin Copyright © 2015 Preeti Jadhav et al. All rights reserved. Keloidal Scleroderma: Case Report and Review Mon, 30 Nov 2015 15:37:23 +0000 http://www.hindawi.com/journals/cridm/2015/635481/ Objective. We report a rare case of keloidal scleroderma and provide an analysis of similar cases. Results. A 41 year-old woman presented with dark brown, indurated, exophytic nodules over the chest along with smaller hyperpigmented plaques scattered over the abdomen, with concomitant sclerodactyly. The clinical, laboratory, and pathological findings were consistent with a diagnosis of keloidal scleroderma. The patient was treated with methotrexate, resulting in reduced firmness of her plaques and no new lesions. A literature review of previously reported cases was performed using keywords including keloidal morphea, keloidal scleroderma, nodular morphea, and nodular scleroderma. In our review, the majority of patients were African American and female. 91% of cases had nodular lesions with distribution on the trunk. The majority of patients exhibited sclerodactyly and pulmonary involvement was reported in 28%1. The majority of patients were ANA positive (63%) and only 10% demonstrated anti-SCL-70 positivity. Conclusion. Keloidal scleroderma is a rare presentation, which can often be clinically confused with keloid and scar formation. Due to this being a rare variant, our knowledge of treatment options and efficacy is limited. Methotrexate could be considered as an initial treatment option for patients with progressive keloidal scleroderma. Sama Kassira, Tarannum Jaleel, Peter Pavlidakey, and Naveed Sami Copyright © 2015 Sama Kassira et al. All rights reserved. A Rare Case of Zosteriform Cutaneous Metastases from a Nasopharyngeal Carcinoma Mon, 30 Nov 2015 09:35:05 +0000 http://www.hindawi.com/journals/cridm/2015/415393/ From a clinical point of view, the most common presentations of cutaneous metastatic disease are papules and nodules. However, a wide morphological spectrum of lesions has been described, including erythematous patches or plaques, inflammatory erysipelas-like lesions, diffuse sclerodermiform lesions with induration of the skin, telangiectatic papulovesicles, purpuric plaques mimicking vasculitis, and alopecia areata like scalp lesions. The so-called zosteriform pattern has been described to be in few cases and to the best of our knowledge has never been described associated with a metastasis of a nasopharyngeal carcinoma. This case highlights the relevance of including cutaneous metastases in the differential diagnosis of patients with nonhealing herpes zoster-like lesions, especially in those with underlying neoplasm recently diagnosed. Andrés González García, Emiliano Grillo Fernández, Ignacio Barbolla Díaz, Asunción Ballester, Héctor Pian, and Guadalupe Fraile Copyright © 2015 Andrés González García et al. All rights reserved. An Uncommon Side Effect of Bupropion: A Case of Acute Generalized Exanthematous Pustulosis Tue, 24 Nov 2015 12:28:36 +0000 http://www.hindawi.com/journals/cridm/2015/421765/ Acute generalized exanthematous pustulosis (AGEP) is a rare inflammatory dermatosis characterized by multiple nonfollicular pustules that occur on erythematous skin. Despite its similarity to pustular psoriasis and association with fever and leukocytosis, AGEP typically heals quickly. Etiologically, drugs and viruses have been suspected in most cases. Here, we present a case of AGEP, in a woman, that developed 1 day after starting bupropion for smoking cessation, as a rare side effect of the treatment. Hasan Tak, Cengiz Koçak, Gülben Sarıcı, Nazlı Dizen Namdar, and Mehtap Kıdır Copyright © 2015 Hasan Tak et al. All rights reserved. A Rare Colocalization of Lichen Planus and Vitiligo Tue, 24 Nov 2015 12:19:17 +0000 http://www.hindawi.com/journals/cridm/2015/840193/ We report an unusual manifestation of vitiligo colocalizing with lichen planus (LP). A 76-year-old Greek male presented with a history of a red, scaly, itchy, asymmetrical patch located at the umbilicus within a well-demarcated depigmented macule of vitiligo. Histology showed features of a lichenoid interface dermatitis, favouring a diagnosis of LP. Colocalization of LP and vitiligo has rarely been reported in the literature. After reviewing the literature, we believe that at present there is insufficient evidence to resolve the uncertainties in the aetiology of this colocalization. It seems to us that the association between LP and vitiligo is more than coincidental, but none of the theories discussed in this paper can sufficiently account for it. Rather, the association is likely to be multifactorial in its pathogenesis. David Veitch, Georgios Kravvas, Sian Hughes, and Christopher Bunker Copyright © 2015 David Veitch et al. All rights reserved. Effectiveness of an Innovative Pulsed Electromagnetic Fields Stimulation in Healing of Untreatable Skin Ulcers in the Frail Elderly: Two Case Reports Sun, 08 Nov 2015 07:32:36 +0000 http://www.hindawi.com/journals/cridm/2015/576580/ Introduction. Recalcitrant skin ulcers are a major burden in elderly patients. Specifically, chronic wounds result in significant morbidity and mortality and have a profound economic impact. Pulsed electromagnetic fields (PEMFs) have proved to be a promising therapy for wound healing. Here we describe the first reported case of an innovative PEMF therapy, Emysimmetric Bilateral Stimulation (EBS), used to successfully treat refractory skin ulcers in two elderly and fragile patients. Case Presentation. Two elderly patients developed multiple chronic skin ulcerations. Despite appropriate treatment, the ulcers showed little improvement and the risk of amputation was high. Both patients underwent daily EBS therapy and standard dressing. After few weeks of treatment, major improvements were observed and all ulcers had healed. Conclusion. In patients with refractory ulceration, EBS therapy may be of real benefit in terms of faster healing. This case supports the supportive role for PEMFs in the treatment of skin ulceration in diabetes and is suggestive of a potential benefit of EBS in this clinical condition. Fabio Guerriero, Emanuele Botarelli, Gianni Mele, Lorenzo Polo, Daniele Zoncu, Paolo Renati, Carmelo Sgarlata, Marco Rollone, Giovannoi Ricevuti, Niccolò Maurizi, Matthew Francis, Mariangela Rondanelli, Simone Perna, Davide Guido, and Piero Mannu Copyright © 2015 Fabio Guerriero et al. All rights reserved. Type VI Aplasia Cutis Congenita: Bart’s Syndrome Sun, 01 Nov 2015 12:51:39 +0000 http://www.hindawi.com/journals/cridm/2015/549825/ Bart’s syndrome is characterized by aplasia cutis congenita and epidermolysis bullosa. We present the case of a newborn male who developed blisters on the mucous membranes and the skin following congenital localized absence of skin. Bart’s syndrome (BS) is diagnosed clinically based on the disorder’s unique signs and symptoms but histologic evaluation of the skin can help to confirm the final diagnosis. The patient was managed conservatively with topical antibacterial ointment and wet gauze dressing. Periodic follow-up examinations showed complete healing. We emphasized that it is important to use relatively simple methods for optimal healing without the need for complex surgical interventions. Ferit Kulalı, Ahmet Yagmur Bas, Yusuf Kale, Istemi Han Celik, Nihal Demirel, and Sema Apaydın Copyright © 2015 Ferit Kulalı et al. All rights reserved. Melanoma of the Right Foot Simulating Kaposi’s Disease Thu, 08 Oct 2015 09:23:22 +0000 http://www.hindawi.com/journals/cridm/2015/750491/ Melanoma is a malignant tumor rarely being described in sub-Saharan Africa. We reported an unusual and atypical clinical presentation. It was a 59-year-old patient who was hospitalized for a monomelic black tumor evolving for 10 years. Histopathological examination confirmed the melanocytic origin of this tumor. Paraclinical assessment did not find any visceral metastasis. A partial resection of the tumor was performed. The patient left the hospital against medical consent due to lack of technical facilities. The delay in the consultation and the lack of knowledge of melanoma by doctors and patients might contribute to the severity and the difficulties of its management. K. A. Kouassi, K. Kassi, K. Kouamé, M. A. Oussou, I. Kouassi, I. P. Gbery, E. J. Ecra, A. Sangare, C. Ahogo, M. Kaloga, P. Yoboue, and J. M. Kanga Copyright © 2015 K. A. Kouassi et al. All rights reserved. Peripheral Ulcerative Keratitis with Pyoderma Gangrenosum Wed, 07 Oct 2015 14:07:23 +0000 http://www.hindawi.com/journals/cridm/2015/949840/ Pyoderma gangrenosum is an unusual necrotizing noninfective and ulcerative skin disease whose cause is unknown. Ophthalmic involvement in pyoderma gangrenosum is an unusual event. Only a few cases have been reported, from which we can highlight scleral, corneal, and orbital cases. Peripheral ulcerative keratitis is a process which destroys the peripheral cornea. Its cause is still unknown although it is often associated with autoimmune conditions. Pyoderma gangrenosum should be included in the differential diagnosis of peripheral ulcerative keratitis. Early recognition of these manifestations can vary the prognosis by applying the appropriate treatment. We introduce a 70-year-old woman who suffered pyoderma gangrenosum associated with peripheral ulcerative keratitis in her left eye. The patient’s skin lesions and peripheral keratitis responded successfully to systemic steroids and cyclosporine A. Adrián Imbernón-Moya, Elena Vargas-Laguna, Antonio Aguilar, Miguel Ángel Gallego, Claudia Vergara, and María Fernanda Nistal Copyright © 2015 Adrián Imbernón-Moya et al. All rights reserved. Pulmonary Tuberculosis and Lepromatous Leprosy Coinfection Sun, 04 Oct 2015 12:30:56 +0000 http://www.hindawi.com/journals/cridm/2015/898410/ Simultaneous occurrence of leprosy and pulmonary tuberculosis is reported infrequently in the modern era. We report a case of pulmonary tuberculosis diagnosed in patient being treated with glucocorticoids for complications of leprosy (type II reaction). Physicians should recognize that the leprosy patients treated with glucocorticoid may develop tuberculosis. F. A. Sendrasoa, I. M. Ranaivo, O. Raharolahy, M. Andrianarison, L. S. Ramarozatovo, and F. Rapelanoro Rabenja Copyright © 2015 F. A. Sendrasoa et al. All rights reserved. Omalizumab for Urticarial Vasculitis: Case Report and Review of the Literature Tue, 08 Sep 2015 11:52:46 +0000 http://www.hindawi.com/journals/cridm/2015/576893/ Urticarial vasculitis is characterised by inflamed itching or burning red patches or wheals that resemble urticaria but persist for greater than 24 hours. It is often idiopathic but is sometimes associated with collagen-vascular disease, particularly systemic lupus erythematosus. Treatment options include oral antihistamines, oral corticosteroids, dapsone, colchicine or hydroxychloroquine. We describe a male patient with urticarial vasculitis who was treated with omalizumab (anti-IgE) with convincing results and provide a review of previous reports of patients with urticarial vasculitis treated with omalizumab. Misbah Nasheela Ghazanfar and Simon Francis Thomsen Copyright © 2015 Misbah Nasheela Ghazanfar and Simon Francis Thomsen. All rights reserved. Reconstruction of a Large Anterior Ear Defect after Mohs Micrographic Surgery with a Cartilage Graft and Postauricular Revolving Door Flap Thu, 03 Sep 2015 11:25:24 +0000 http://www.hindawi.com/journals/cridm/2015/484819/ A novel postauricular revolving door island flap and cartilage graft combination was employed to correct a large defect on the anterior ear of an 84-year-old man who underwent Mohs micrographic surgery for an antihelical squamous cell carcinoma. The defect measured 4.6 × 2.4 cm and spanned the antihelix, scapha, a small portion of the helix, and a large segment of underlying cartilage, with loss of structural integrity and anterior folding of the ear. The repair involved harvesting 1.5 cm2 of exposed cartilage from the scaphoid fossa and then sculpting and suturing it to the remnant of the antihelical cartilage in order to recreate the antihelical crura. The skin of the posterior auricle was then incised just below the helical rim and folded anteriorly to cover the cartilage graft. The flap remained attached by a central subcutaneous pedicle, and an island designed using the full-thickness defect as a stencil template was pulled through the cartilage window anteriorly to resurface the anterior ear. This case demonstrates the use of the revolving door flap for coverage of large central ear defects with loss of cartilaginous support and illustrates how cartilage grafts may be used in combination with the flap to improve ear contour after resection. Stephanie Nemir, Lindsey Hunter-Ellul, Vlad Codrea, and Richard Wagner Copyright © 2015 Stephanie Nemir et al. All rights reserved. Buschke-Löwenstein Tumour: Successful Treatment with Minimally Invasive Techniques Mon, 31 Aug 2015 08:30:06 +0000 http://www.hindawi.com/journals/cridm/2015/651703/ We report a case of an 80-year-old female who presented with a four-year history of a growing mass in the perianal area with pain and bleeding during defaecation. Clinical examination revealed a locally destructive, cauliflower-like, verrucous mass measuring 10 12 cm in diameter. Histologic findings revealed a moderate degree of dysplasia of the epithelium with koilocytosis atypia, acanthosis, and parakeratosis, features that are consistent with Buschke-Löwenstein tumour. Polymerase-chain-reaction assay for human papillomavirus (HPV) showed an infection with HPV type 11. Full-thickness excision of involved skin was undertaken by cryotherapy and electrocautery over five months. The entire wound was left open to heal by secondary intention. After 3 years of follow-up, the patient has not experienced a recurrence, with excellent functional results, but the cosmetic results were satisfactory. These minimally invasive techniques can be safer and more cost-effective than surgery and the General Practitioner can play a key role in diagnosis. Estefânia Correia and António Santos Copyright © 2015 Estefânia Correia and António Santos. All rights reserved. Methotrexate Treatment in Children with Febrile Ulceronecrotic Mucha-Habermann Disease: Case Report and Literature Review Thu, 27 Aug 2015 13:23:35 +0000 http://www.hindawi.com/journals/cridm/2015/357973/ Febrile Ulceronecrotic Mucha-Habermann disease is a rare and potentially fatal variant of pityriasis lichenoides et varioliformis acuta and is characterized by high fever, constitutional symptoms, and acute oncet of ulceronecrotic lesions. We present an 11-year-old male with Febrile Ulceronecrotic Mucha-Habermann disease who was cured with methotrexate and review the use of methotrexate for this disorder in the pediatric age group with the relevant literature. Isil Bulur, Hilal Kaya Erdoğan, Zeynep Nurhan Saracoglu, and Deniz Arık Copyright © 2015 Isil Bulur et al. All rights reserved. Case of Rapid Progression of Hemiatrophy on the Face: A New Clinical Entity? Tue, 25 Aug 2015 10:59:01 +0000 http://www.hindawi.com/journals/cridm/2015/478640/ A lot of diseases, including lupus profundus, morphea, lipodystrophy, and Parry-Romberg syndrome, may manifest progressive hemifacial atrophy. These diseases usually progress slowly and rapid progression of atrophy is extremely rare. We report a case of elderly-onset rapid progression of hemifacial atrophy only in three weeks. Our case did not meet variable differential diagnoses. We discuss the clinical character of the patient against the past of literature and suppose it may be a new clinical entity. Hisashi Nomura, Shohei Egami, Tomoaki Yokoyama, and Makoto Sugiura Copyright © 2015 Hisashi Nomura et al. All rights reserved. Lymphatic Malformation, Retinoblastoma, or Facial Cleft: Atypical Presentations of PHACE Syndrome Sun, 28 Jun 2015 11:39:52 +0000 http://www.hindawi.com/journals/cridm/2015/487562/ PHACE syndrome is a neurocutaneous disorder characterized by large cervicofacial infantile hemangiomas and associated anomalies: posterior fossa brain malformation, hemangioma, arterial cerebrovascular anomalies, coarctation of the aorta and cardiac defects, and eye/endocrine abnormalities of the brain. When ventral developmental defects (sternal clefting or supraumbilical raphe) are present the condition is termed PHACE. In this report, we describe three PHACE cases that presented unique features (affecting one of the organ systems described for this syndrome) that have not been described previously. In the first case, a definitive PHACE association, the patient presented with an ipsilateral mesenteric lymphatic malformation, at the age of 14 years. In the second case, an anomaly of the posterior segment of the eye, not mentioned before in PHACE literature, a retinoblastoma, has been described. Specific chemotherapy avoided enucleation. And, in the third case, the child presented with an unusual midline frontal bone cleft, corresponding to Tessier 14 cleft. Two patients’ hemangiomas responded well to propranolol therapy. The first one was followed and treated in the pre-propranolol era and had a moderate response to corticoids and interferon. María Fernández-Ibieta and Juan Carlos López-Gutiérrez Copyright © 2015 María Fernández-Ibieta and Juan Carlos López-Gutiérrez. All rights reserved. Clinical Effects of Topical Tacrolimus on Fox-Fordyce Disease Mon, 15 Jun 2015 07:07:42 +0000 http://www.hindawi.com/journals/cridm/2015/205418/ Fox-Fordyce Disease (FFD) is a rare, chronic, pruritic, inflammatory disorder of apocrine glands. It is characterized by dome-shaped, firm, discrete, skin-colored, and monomorphic perifollicular papules. The most common sites of involvement are axillae and anogenital and periareolar regions which are rich in apocrine sweat glands. Treatment is difficult. Topical, intralesional steroids, topical tretinoin, adapalene, clindamycin, benzoyl peroxide, oral contraceptives, isotretinoin, phototherapy, electrocauterisation, excision-liposuction and curettage, and fractional carbon dioxide laser are among the treatment options. In the literature, there are articles reporting beneficial effects of pimecrolimus in FFD. Nevertheless, there have not been any reports about the use of tacrolimus in FFD. We report two patients diagnosed with FFD by clinical and histopathologic examination and discussed therapeutic effects of topical tacrolimus on FFD in the light of literature. Hilal Kaya Erdoğan, Işıl Bulur, and Zeliha Kaya Copyright © 2015 Hilal Kaya Erdoğan et al. All rights reserved. Subcutaneous Emphysema Induced by Cryotherapy: A Complication due to Previous Punctures Wed, 10 Jun 2015 12:51:39 +0000 http://www.hindawi.com/journals/cridm/2015/374817/ Cryosurgery is a common therapeutic modality used in dermatology; therefore we must be aware of its possible adverse effects. We report a case of a patient with subcutaneous emphysema which occurred following the application of cryotherapy after multiple punctures of local anesthetic and intralesional steroids in a chest keloid scar. Despite the fact that this condition was gradually resolved after expectant observation, we warn about this complication when sprayed cryotherapy is preceded by multiple punctures on cutaneous lesions above bony surfaces. In similar settings, cryotherapy must be first administered or a cotton-tip applicator should be used. Jared Martínez-Coronado, Bertha Torres-Álvarez, and Juan Pablo Castanedo-Cázares Copyright © 2015 Jared Martínez-Coronado et al. All rights reserved. Staphylococcal Scalded Skin Syndrome in Neonate Mon, 08 Jun 2015 08:12:13 +0000 http://www.hindawi.com/journals/cridm/2015/901968/ We described a case of Staphylococcal Scalded Skin Syndrome in infant age of 21 days by discussing clinical and management issues. This newborn presented large erythematous, eroded, and oozing areas covered by epidermal skin flap. The average surface of cutaneous unsticking on admission was 31.35% of body surface area corresponding to lesions of superficial second-degree burns. An important biological inflammatory syndrome including positive C-reactive protein was found. Under treatment, erythroderma decreased within 7 to 10 days and the newborn was completely healed after 3 weeks of followup, with the disappearance of the inflammatory syndrome and total body surface restored. This clinical case report showed that SSSS remains a major dermatological problem in neonates. Therefore, its diagnosis should be made without doubt and its care should start earlier in a neonate emergency unit in order to have good prognosis. And the rigorous “search and destroy” policy based on screening of staff and patients and isolation of identified patients advocated in the United Kingdom should be applied in neonate units in Côte d’Ivoire. K. Kouakou, M. E. Dainguy, and K. Kassi Copyright © 2015 K. Kouakou et al. All rights reserved. Paget Disease of the Vulva: Diagnosis by Immunohistochemistry Tue, 28 Apr 2015 08:11:56 +0000 http://www.hindawi.com/journals/cridm/2015/162483/ The objective of this paper is to report a case of extramammary Paget disease of the vulva, to describe its diagnosis, surgical treatment, and outcome, and to discuss the general characteristics of this pathology. This is a rare neoplasm, found principally in areas in which apocrine and eccrine glands are numerous. This case report is relevant to the literature since the differential diagnosis of extramammary Paget disease is difficult to be done only with the macroscopic appearance of the lesion and even with the microscopic characteristics, requiring further studies, immunohistochemistry, as to differentiate pathologies. The present report describes the case of a 63-year-old patient at the Santa Casa de Misericórdia Hospital in Vitória, Espírito Santo, Brazil, who presented with a hardened, ulcerated, and purplish lesion with hyperchromic and hypochromic spots, measuring 4 cm in diameter, located on the lower third of right labium majus, close to the vaginal fourchette. A right hemivulvectomy was performed, leaving wide margins all around. The patient progressed satisfactorily following surgery. Although extramammary Paget disease is rare, its incidence increases as a function of the patient’s age. Patients should be followed up closely because of the risk of persistence and/or recurrence of the disease. Andressa Gonçalves Amorim, Brunelle Batista Fraga Mendes, Rodrigo Neves Ferreira, and Antônio Chambô Filho Copyright © 2015 Andressa Gonçalves Amorim et al. All rights reserved. Two Basal Cell Carcinomas of the Axillae: A Metastasis or an Independent Development? Sun, 15 Mar 2015 11:28:46 +0000 http://www.hindawi.com/journals/cridm/2015/637292/ Cutaneous basal cell carcinoma (BCC) is a common malignancy amongst the elderly. BCC rarely metastasises, and fewer than 300 cases of metastatic BCC have been reported in the literature. Here, we report a case of sequentially developed BCCs located adjacent to each other. We discuss that these BCCs were considered to have developed independently rather than due to metastasis, after referencing previous studies on metastatic BCC. Yuichiro Endo and Yoshiki Miyachi Copyright © 2015 Yuichiro Endo and Yoshiki Miyachi. All rights reserved. Perianal Median Raphe Cyst: A Rare Lesion with Unusual Histology and Localization Sun, 22 Feb 2015 07:37:15 +0000 http://www.hindawi.com/journals/cridm/2015/487814/ Median raphe cysts present anywhere between the external urethral meatus and the anus. The cysts can occur at parameatus, glans penis, penile shaft, scrotum, or perineum. Perianal region is an extremely rare location for these lesions. Here we present a 50-year-old male patient who presented with a cystic, fluctuant lesion, located at 12 o’clock in perianal region. Microscopic examination revealed a cystic lesion with keratinized and nonkeratinized stratified squamous epithelium, pseudostratified ciliated epithelium, and scattered goblet cells. The final diagnosis of the lesion was median raphe cyst. Ciliated cells and perianal localization in median raphe cysts are extremely rare characteristics. Betül Ünal, Cumhur İbrahim Başsorgun, Meryem İlkay Eren Karanis, and Gülsüm Özlem Elpek Copyright © 2015 Betül Ünal et al. All rights reserved. Etanercept-Induced Pityriasis Lichenoides Chronica in a Patient with Rheumatoid Arthritis Wed, 18 Feb 2015 11:56:54 +0000 http://www.hindawi.com/journals/cridm/2015/168063/ We present a 74-year-old female patient who developed a pityriasis lichenoides chronica (PLC) during etanercept therapy. This association is not described in the literature and might be considered in the spectrum of cutaneous adverse reactions of etanercept. Andrés F. Echeverri, Andrés Vidal, Carlos A. Cañas, Andrés Agualimpia, Gabriel J. Tobón, and Fabio Bonilla-Abadía Copyright © 2015 Andrés F. Echeverri et al. All rights reserved. A Case of Recalcitrant Plantar Warts Associated with Statin Use Wed, 18 Feb 2015 09:47:06 +0000 http://www.hindawi.com/journals/cridm/2015/320620/ Background. Plantar warts are a common presenting skin complaint caused by the human papillomavirus. 1st line therapies include cryotherapy and topical salicylic acid. Where there is resistance to these treatments, consideration is made for 2nd line therapies, including intralesional bleomycin, imiquimod, 5-fluorouracil, and photodynamic therapy. We present a case of bilateral persistent plantar warts, resistant to treatment with repeated cryotherapy and topical salicylic acid over a 6-year period. Following a patient initiated decision to discontinue their statin medication, we observed rapid clearance of plantar warts without change to standard therapy or their environment. This case correlates with emerging literature demonstrating a link between statin medication and proliferation of HPV through increased levels of FOXP3+ regulatory T cells. Aaron G. Wernham and Shireen S. Velangi Copyright © 2015 Aaron G. Wernham and Shireen S. Velangi. All rights reserved. Mixed Cutaneous Infection Caused by Mycobacterium szulgai and Mycobacterium intermedium in a Healthy Adult Female: A Rare Case Report Wed, 18 Feb 2015 09:18:14 +0000 http://www.hindawi.com/journals/cridm/2015/607519/ Nontuberculous mycobacteria (NTMs) are ubiquitous and are being increasingly reported as human opportunistic infection. Cutaneous infection caused by mixed NTM is extremely rare. We encountered the case of a 46-year-old female, who presented with multiple discharging sinuses over the lower anterior abdominal wall (over a previous appendectomy scar) for the past 2 years. Microscopy and culture of the pus discharge were done to isolate and identify the etiological agent. Finally, GenoType Mycobacterium CM/AS assay proved it to be a mixed infection caused by Mycobacterium szulgai and M. intermedium. The patient was advised a combination of rifampicin 600 mg once daily, ethambutol 600 mg once daily, and clarithromycin 500 mg twice daily to be taken along with periodic follow-up based upon clinical response as well as microbiological response. We emphasize that infections by NTM must be considered in the etiology of nonhealing wounds or sinuses, especially at postsurgical sites. Amresh Kumar Singh, Rungmei S. K. Marak, Anand Kumar Maurya, Manaswini Das, Vijaya Lakshmi Nag, and Tapan N. Dhole Copyright © 2015 Amresh Kumar Singh et al. All rights reserved. Unilateral Oral Mucous Membrane Pemphigoid: Refractory Atypical Presentation Successfully Treated with Intravenous Immunoglobulins Sun, 15 Feb 2015 06:48:51 +0000 http://www.hindawi.com/journals/cridm/2015/930859/ A 57-year-old male presented with a 6-month history of blisters and painful erosions on the right buccal mucosa. No skin or other mucosal involvement was seen. The findings of histopathological and direct immunofluorescence examinations were sufficient for the diagnosis of oral mucous membrane pemphigoid in the context of adequate clinical correlation. No response was seen after topical therapies and oral corticosteroids or dapsone. Intravenous immunoglobulin was started and repeated every three weeks. Complete remission was achieved after three cycles and no recurrence was seen after two years of follow-up. The authors report a rare unilateral presentation of oral mucous membrane pemphigoid on the right buccal and hard palate mucosa, without additional involvement during a period of five years. Local trauma or autoimmune factors are possible etiologic factors for this rare disorder, here with unique presentation. André Laureano and Jorge Cardoso Copyright © 2015 André Laureano and Jorge Cardoso. All rights reserved. Harmful Effects of Synthetic Surface-Active Detergents against Atopic Dermatitis Thu, 15 Jan 2015 06:21:03 +0000 http://www.hindawi.com/journals/cridm/2015/898262/ We report herein two cases of intractable atopic dermatitis successfully treated by simply avoiding the contact with surface-active detergents in the daily life and living. The detergents were closely related to the exacerbation and remission of the disease. Steroid ointment was no longer used. We discuss that the removal of horny layer lipids by surface-active detergents accelerates the transepidermal water loss and disturbs the barrier function of the epidermis and thus is intimately involved in the pathogenesis of atopic dermatitis. Hajime Deguchi, Riho Aoyama, Hideaki Takahashi, Yoshinari Isobe, and Yutaka Tsutsumi Copyright © 2015 Hajime Deguchi et al. All rights reserved. Acquired Brachial Cutaneous Dyschromatosis in a 60-Year-Old Male: A Case Report and Review of the Literature Wed, 31 Dec 2014 08:43:29 +0000 http://www.hindawi.com/journals/cridm/2014/452720/ Acquired brachial cutaneous dyschromatosis is an acquired pigmentary disorder that has been described in only 20 patients but likely affects many more. This case of a man with acquired brachial cutaneous dyschromatosis is unique as most reports are in women. We report the case of a 60-year-old male who presents with an asymptomatic eruption characterized by hyperpigmented and telangiectatic macules coalescing into patches on the bilateral extensor aspects of the forearms which is consistent clinically and histopathologically with acquired brachial cutaneous dyschromatosis. Given its presence in patients with clinical evidence of chronic sun exposure and its histopathological finding of solar elastosis, acquired brachial cutaneous dyschromatosis is likely a disorder caused by cumulative UV damage. However, a possible association between angiotensin-converting enzyme inhibitors and acquired brachial cutaneous dyschromatosis exists. Further investigation is needed to elucidate both the pathogenesis of the disorder and forms of effective management. Treatment of the disorder should begin with current established treatments for disorders of dyspigmentation. Nadia Abidi, Kristen Foering, and Joya Sahu Copyright © 2014 Nadia Abidi et al. All rights reserved.