A present a clinical case of a rare variant of dermatofibroma (aneurysmatic type), is presented in a 72-year-old female patient, the lesion was located in the right arm’s flexural fold, resulting from mesenchymal proliferation associated with blood vessels and tissular hemorrhage, with its own well defined histological characteristics. The objectives are to describe the rarity of the lesion and its histopathologic importance, when compared to other benign and malignant tumors in the differential diagnosis, in addition to the terminology currently used.

Keywords: BENIGN FIBROUS HISTIOCYTOMA, MALIGNANT FIBROUS HISTIOCYTOMA, HEMOSIDERIN

The present paper describes the case of a 47-year-old female patient, with discoid lupus erythematosus-the most common clinical variant of chronic cutaneous lupus-presenting achromic cicatricial lesions on the face. The punch grafting technique was performed in the following regions: right supraorbital, right malar, and nasal. The donor sites were the left and right retroauricular regions. A repigmentation halo of about 1cm was observed around each graft. This technique has been used in the treatment of refractory vitiligo, however it can also be used in inactive achromic cicatricial lesions of discoid lupus with good results.

Keywords: LUPUS ERYTHEMATOSUS, DISCOID; SKIN TRANSPLANTATION; AMBULATORY SURGICAL PROCEDURES; SKIN.

The solitary dermatofibroma or benign superficial fibrous histiocytoma is a common tumor that arises in the lower limbs of young women. Multiple eruptive dermatofibromas constitute a rare presentation of dermatofibromas (0.3%), often associated with underlying diseases. They are defined by the presence of 15 or more lesions or the appearance of five to eight tumors within less than four months. On PubMed/MEDLINE, to date, there are about 40 published cases of multiple eruptive dermatofibromas related to systemic diseases such as systemic lupus erythematosus, Sjögren's syndrome, hepatitis C, AIDS and the use of imunossupressants. The authors report a case where the emergence of multiple eruptive dermatofibromas preceded the onset of systemic lupus erythematosus by 20 years.

Keywords: HISTIOCYTOMA, BENIGN FIBROUS; LUPUS ERYTHEMATOSUS, SYSTEMIC; IMMUNOSUPPRESSIVE AGENTS.

Eccrine spiradenoma is a rare benign adnexal epithelial neoplasm characterized by a bluish-pink, slow-growing solitary nodule, coursing with paroxysmal pain, mainly in young adults. It is most commonly located in the trunk and extremities. Bleeding and/or ulceration are common in the giant vascular variant, which is characterized by a size greater than 2 cm in diameter and a high degree of vascularization seen on histology. Its clinical characteristics are unspecific and require biopsy with histological analysis for diagnosis. Its histology presents one or more basophilic intradermal lobules enveloped in a fibrous capsule without connection to the epidermis. It presents two types of cells: small cells with dark nuclei in the periphery and large cells with light nuclei in the center. An accurate diagnosis is important due to the fact that it can develop into a potentially fatal malignancy - which is a rare phenomenon and occurs most often in the multiple variant. A rare case of eccrine spiradenoma in the abdomen with bleeding associated is described in the present paper, as well as a discussion on possible treatments.

Keywords: ECCRINE SPIROADENOMA, BENIGN EPITHELIAL NEOPLASIA, SEBACEOUS GLANDS

The present paper describes the case of a 47 year-old patient with facial Lupus Panniculitis, with absence of disease activity in excess of one year. The large malar and temporomandibular atrophy caused by the pathology has become a great problem for the patient, with impacts on her quality of life. A cutaneous filling procedure was carried out with hyaluronic acid using microcannulas, compensating the defect and with aesthetically appropriate results.

Keywords: CHYALURONIC ACID; PANNICULITIS, LUPUS ERYTHEMATOSUS; QUALITY OF LIFE

The Hailey-Hailey disease or familial benign pemphigus is a rare condition, characterized by vesicular lesions and erosions with a predilection for intertriginous areas associated with pain and burning sensation that affect the quality of life of patients. There are many topical and systemic treatments for the injuries that can temporarily promote partial or complete remission, but there is no curative treatment. Some treatment options with lasting results include dermabrasion and Erbium laser resurfacing (YAG or CO2). We report three cases of patients with recurrent lesions and limited responses to classical treatments, which showed significant clinical improvement after fractional CO₂ laser therapy.

Keywords: PEMPHIGUS, BENIGN FAMILIAL; LASER THERAPY; CARBON DIOXIDE

Aneurysmal dermatofibroma (DF) is a rare benign tumor originating in the dermis, considered a variant of dermatofibroma. It is more prevalent in women over 30 years of age, in the lower limbs. Its etiology is unknown and histopathological examination confirms the diagnosis. This study reports two cases of aneurysmal DF in young patients, both men, presenting similar lesions: single hyperchromic nodule, with approximately 1.5 cm and progressive growth. This report aims to demonstrate an uncommon variant of dermatofibroma and to highlight the possible differential diagnosis with other tumors through dermoscopic examination.

Keywords: Dermoscopy; Histiocytoma, Benign Fibrous; Dermatology

Malignant fibrous histiocytoma (MFH) or undifferentiated pleomorphic sarcoma (UPS) is a sarcoma capable of invading adjacent structures. It is a mesenchymal neoplasia that predominates in men between the sixth and seventh decades of life. It is located mainly in the lower limbs and may affect the head and neck, trunk, and retroperitoneum, presenting a tendency to recurrence and local metastasis. This report aims to present a case of MFH in the ankle of a 49-year-old woman with an adjacent bone invasion, which evolved with transtibial amputation. Clinical, radiological, histopathological, and therapeutic aspects were addressed, highlighting the importance of early diagnosis.

Keywords: Amputation; Malignant fibrous histiocytoma; Sarcoma

Aneurysmal dermatofibroma (ADF) is a rare benign tumor originating in the dermis. It is most common in the lower limbs of women over 30 years. Its etiology is unknown, and histopathological examination confirms the diagnosis. This paper presents a case of ADF with an exuberant presentation in a young female patient with a pedunculated tumor in the right pretibial region, measuring 12 cm in greatest diameter. This report aims to demonstrate an infrequent variant of dermatofibroma with significant growth and emphasize the importance of lesion excision and follow-up because of the high recurrence rate.

Keywords: Histiocytoma, Benign fibrous; Dermatology; Dermoscopy

INTRODUCTION: The advent of squamous cell carcinomas (SCC) from chronic dermatoses is known but little explored. Although rare, tumors originating there have a worse prognosis, in part due to late diagnosis.
OBJECTIVES: This study aims to survey cases of squamous cell carcinoma developed on previous dermatoses diagnosed between 2000 and 2020 in a tertiary health service.
METHODS: This is a quantitative and retrospective study through biopsy reports survey and medical records review.
RESULTS: From an initial list of 11,249 histological reports compatible with squamous cell carcinoma, we obtained a final list of 10 patients. The study findings corroborate the literature regarding some known risk factors: abundant and chronic sun exposure, older than 50 years, lower skin phototypes, and immunosuppression. We also found a high frequency of smoking and lichenoid dermatoses (5/10 patients) in the studied population, including chronic cutaneous lupus erythematosus and hypertrophic lichen planus.
CONCLUSIONS: It is not possible to predict the primary risk factors for the development of squamous cell carcinomas regarding previous dermatoses, although there is a tendency for their appearance in lichenoid dermatoses and those with longer evolution.

Keywords: Skin diseases; Squamous cell carcinoma; Lupus erythematosus, Cutaneous; Lichen planus

Discoid lupus erythematosus (DLE) causes chronic lesions that can heal with dyschromic patches. We report a clinical case showing success in the treatment of achromic lesions using a combination of surgical techniques, including excision, punch grafting, and full-thickness skin grafting.

Keywords: Lupus Erythematosus, Discoid; Cicatrix; Surgical Procedures, Operative.