journal
https://read.qxmd.com/read/38601048/thoracocervicofacial-purpura-as-a-presenting-symptom-of-seizure-disorder-a-case-report
#1
Waseem Alhawsawi, Khalid Al Hawsawi, Alhusain Alshareef, Rama Halabi, Ammar Baksh, Basant Alzubaidy
INTRODUCTION: Postictal thoracocervicofacial purpura (PTP) is a rare clinical sign after a seizure episode and may be the only objective sign seen in patients who are unaware of their own seizure disorder. Moreover, it can be the only reason a patient seeks medical care after a seizure activity. CASE PRESENTATION: Herein, we report a 23-year-old, living alone and not known to have any medical illnesses, who presented to our emergency department complaining of asymptomatic purpuric facial rash extending to his neck and upper chest that started suddenly when he woke up that morning...
2024: Case Reports in Dermatology
https://read.qxmd.com/read/38590388/efficacy-of-siltuximab-and-1-927-nm-fractional-laser-for-the-treatment-of-cutaneous-manifestations-in-castleman-s-disease-the-role-of-dermoscopy-and-reflectance-confocal-microscopy-for-lesion-evaluation
#2
Giovanni Paolino, Marco Ardigò, Emanuel Della-Torre, Luca Moroni, Nathalie Rizzo, Matteo Riccardo Di Nicola, Vittoria Giulia Bianchi, Lorenzo Dagna, Giuseppe Alvise Ramirez, Santo Raffaele Mercuri
INTRODUCTION: Multicentric Castleman's disease (MCD) with cutaneous involvement has rarely been discussed in dermatologic literature, with few reports. Cutaneous lesions in MCD may induce deep scars, causing a significant impact in the daily life of the patients. The treatment of Castleman's disease (CD) is usually a challenge, especially in case of cutaneous involvement. CASE PRESENTATION: We report the case of a 35-year-old Caucasian man with a 3-year-old history of MCD with cutaneous involvement that we treated with a combined therapy characterized by siltuximab and 1,927 nm fractional laser...
2024: Case Reports in Dermatology
https://read.qxmd.com/read/38567034/the-cystic-sponge-anus
#3
Hessel H van der Zee, Pim Aarts
INTRODUCTION: A peculiar spongy appearance of the perianal skin was observed in a patient who underwent wide excision surgery for inguinal and gluteal hidradenitis suppurativa (HS). CASE PRESENTATION: This peculiar appearance was observed in a 62-year-old male patient. It included multiple orifices and cavities forming the spongy aspect of the perianal skin with multiple cysts and giant comedones. The perianal lesions were asymptomatic and the patient had never received any perianal treatment for the comedones or cysts...
2024: Case Reports in Dermatology
https://read.qxmd.com/read/38550795/expanding-the-differential-diagnosis-of-the-painful-nail-a-case-of-an-onychopapilloma-with-neuroma
#4
Jade Conway, Cynthia M Magro, Shari R Lipner
INTRODUCTION: Onychopapilloma most commonly presents as longitudinal erythronychia, but diagnosis may be challenging in some cases due to varied clinical presentations. Most patients with onychopapillomas do not report associated pain but instead more commonly report functional interference. CASE REPORT: We present a case of a 74-year-old female with a 5-year history of splitting and lifting of the right thumbnail, accompanied by nail sensitivity and intermittent painful throbbing...
2024: Case Reports in Dermatology
https://read.qxmd.com/read/38529513/diffuse-lichen-planopilaris-masquerading-as-diffuse-alopecia-areata
#5
Li Jie Helena Yoo, Nekma Meah, Dmitri Wall, Ian McDonald
INTRODUCTION: Lichen planopilaris (LPP) is a primary lymphocytic cicatricial alopecia that represents a form of follicular lichen planus. CASE PRESENTATION: We describe a case of coexisting diffuse LPP and female pattern hair loss masquerading as diffuse alopecia areata in a 32-year-old female. DISCUSSION: In complex cases such as this, dermoscopy-guided vertical and horizontal biopsies from androgen sensitive and insensitive areas are helpful in increasing diagnostic yield...
2024: Case Reports in Dermatology
https://read.qxmd.com/read/38481563/repair-of-a-large-nasal-ala-and-medial-cheek-defect-case-report
#6
Hannah E Myers, Ashley A Kessler, Michael Roberts, Christopher Buckley
INTRODUCTION: Mohs micrographic surgery is a complex but essential aspect of functional and cosmetic skin cancer removal. It allows for skin cancers to be removed from cosmetically challenging areas in the most efficient and effective possible method; however, closure of these lesions can be difficult. CASE: An 80-year-old male presented for Mohs surgery of a basal cell carcinoma on the right nasal sidewall that measured 3.4 cm. The patient underwent seven stages of Mohs surgery, and the final defect measured 6...
2024: Case Reports in Dermatology
https://read.qxmd.com/read/38481562/management-of-locally-advanced-basal-cell-carcinoma-with-sonic-hedgehog-pathway-targeted-therapy-a-case-report-and-discussion
#7
Neal Ferrin, Darwin Edmond, Ryan Jones, Laurence E McCahill
INTRODUCTION: Basal cell carcinoma (BCC) is the most common skin malignancy in the world. While most lesions are treated using surgical methods, others may present as locally advanced or metastatic disease and are not amenable to surgical therapy alone. Treatment with sonic hedgehog pathway inhibitors (vismodegib, sonidegib) is designed to inhibit key signaling proteins and gene pathways involved with BCC to reduce the uncontrolled proliferation of basal cells in complicated disease and can be invaluable in treating patients with advanced disease...
2024: Case Reports in Dermatology
https://read.qxmd.com/read/38440721/comprehensive-treatment-of-a-rare-case-of-complete-primary-pachydermoperiostosis-with-large-facial-keloid-scars-a-case-report-and-literature-review
#8
Haibo Zhao, Jianglin Zhang, Renliang He, Linlin Bao
INTRODUCTION: Pachydermoperiostosis (PDP), or primary hypertrophic osteoarthropathy, is a rare autosomal dominant disease with primary clinical features of pachydermia (thickening of skin) and periostosis (new bone formation). Keloid scar formation is also rather obscure, and some scientists have claimed that keloid scars contain an excessive amount of fibroblasts compared with normal skin as well as a dense mass of irregularly deposited connective tissues. CASE PRESENTATION: A 25-year-old man exhibited extensive skin folding on his face, a gyrus-like scalp, depressed nasolabial folds, and keloids...
2024: Case Reports in Dermatology
https://read.qxmd.com/read/38406644/netherton-syndrome-with-a-novel-likely-pathogenic-variant-c-420del-p-ser141profster5-in-spink5-gene-a-case-report
#9
Katya Kovacheva, Zornitza Kamburova, Preslav Vasilev, Ivelina Yordanova
INTRODUCTION: Netherton syndrome (NS) is a rare autosomal recessive genodermatosis in the group of congenital ichthyosis. The clinical manifestations of the syndrome vary from a very mild clinical manifestation occurring with the picture of ichthyosis linearis circumflexa to exfoliative erythroderma. It can be fatal in the first days of a newborn's life due to dehydration, hypothermia, weight loss, respiratory infections, and sepsis. A specific anomaly of the hair trichorrexis invaginata is considered pathognomonic for the syndrome...
2024: Case Reports in Dermatology
https://read.qxmd.com/read/38406643/lucio-phenomenon-an-unusual-case-of-skin-necrosis
#10
Kaveri Rusia, Vikrant Saoji, Bhushan Madke, Adarshlata Singh
INTRODUCTION: Lucio leprosy is a non-nodular diffuse type of lepromatous leprosy first described by Lucio and Alvarado. Lucio phenomenon is a rare vasculonecrotic reaction characterized by cutaneous necrosis with minimal constitutional features. CASE PRESENTATION: We describe an unusual case of a 53-year-old man from Central India who had blisters, ulcers, and widespread erosions on his foot, forearms, and arms. The diagnosis of lepromatous leprosy with the Lucio phenomenon was established after thorough evaluation by clinical findings, histopathological findings, and slit-skin smear examination...
2024: Case Reports in Dermatology
https://read.qxmd.com/read/38384677/atezolizumab-induced-acrodermatitis-and-pustular-psoriasis-in-a-patient-with-non-small-cell-lung-cancer-a-rare-case-report
#11
Davide Fattore, Gianluca Esposito, Ludovica Carangelo, Maria Antonietta Luciano, Matteo Megna
INTRODUCTION: Immune checkpoint inhibitors are new drugs approved for the treatment of many types of malignancies. Despite their wide use and unquestionable clinical benefits, these agents have also been associated with a unique spectrum of side effects known as immune-related adverse events. In this study, we report the first case of atezolizumab-induced pustular psoriasis and acrodermatitis. CASE PRESENTATION: A 61-year-old woman presented to our department with erythematous-desquamative and pustular lesions involving all hands and feet fingers, inguinal region, and trunk, associated to severe psoriatic onychodystrophy...
2024: Case Reports in Dermatology
https://read.qxmd.com/read/38370392/this-mite-surprise-you-scabies-masquerading-as-langerhans-cell-histiocytosis-a-case-report
#12
Sara Al Janahi, Raghda Al Maashari, Tausif Saleem
INTRODUCTION: Scabies is a common parasitic infestation caused by the mite Sarcoptes scabiei. Scabies can mimic other entities clinically, resulting in misdiagnosis. The presence of a mite in the stratum corneum on biopsy specimens is diagnostic of scabies. However, there are instances when mites are not visible, and immunohistochemical (IHC) staining may be misleading. An example is when IHC demonstrates Cluster of Differentiation 1a and S100 positivity. The main differential diagnosis for this finding is Langerhans cell histiocytosis, a group of idiopathic disorders of bone marrow-derived Langerhans cells, with manifestations ranging from isolated to life-threatening multisystem disease...
2024: Case Reports in Dermatology
https://read.qxmd.com/read/38298760/interesting-mucocutaneous-manifestations-in-covid-19-infection-or-vaccination-confirmed-by-histopathology-a-case-series
#13
JOURNAL ARTICLE
Arash Pour Mohammad, Elahe Noroozi, Milad Gholizadeh Mesgarha, Nasrin Shayanfar, Azadeh Goodarzi
INTRODUCTION: Mucocutaneous complications or adverse events due to SARS-CoV-2 infection or vaccination have been well delineated in the literature, respectively. Most eruptions are considered mild and self-limiting; however, for the atypical cases with a tentative clinical diagnosis, performing a biopsy and histopathological assessment is pivotal to confirm the diagnosis and subsequently prescribe a more tailored treatment. Despite the diverse reporting of such incidents globally, most studies restrict the rate of biopsied cases to less than 15%...
2024: Case Reports in Dermatology
https://read.qxmd.com/read/38196704/dermoscopic-features-of-heterotopic-salivary-gland-tissue-in-the-neck-report-of-a-case
#14
Shinichiro Inoue, Takuya Maeda, Yuri Nagata, Teruki Yanagi, Hideyuki Ujiie
INTRODUCTION: Heterotopic salivary gland tissue (HSGT) is diagnosed when salivary gland tissue is found in areas other than the major or minor salivary glands. No dermoscopic findings of HSGT have been reported. CASE PRESENTATION: This case report gives the dermoscopic findings of a 45-year-old woman with HSGT who presented with a longstanding pale red macule on her neck, characterized by repeated clear fluid discharge. Dermoscopic examination showed a red dot with a pale pink halo and telangiectasia throughout the lesion...
2024: Case Reports in Dermatology
https://read.qxmd.com/read/38188892/parascapular-flap-for-severe-hidradenitis-suppurativa
#15
Saad Khayat, Nuria Bonsfills, Raúl Antúnez-Conde, Sara Álvarez-Mokthari, Hubert Aranibar, Manuel Tousidonis, Mario Fernández-Fernández, Alberto Díez-Montiel
Hidradenitis suppurativa is a chronic inflammatory disease which affects apocrine glands and hair follicles of the skin, primarily in the axillary and groin regions. This condition can be highly debilitating, causing painful lesions and a negative psychological impact on patients. While medical and minimally invasive treatments are available, surgical intervention may be necessary for severe cases. In cases involving axillary defects, the use of local flaps such as the parascapular flap is a viable option. In this case report, we present a 34-year-old woman who presented to our clinic with a history of recurrent abscesses and cutaneous infections in the axillary region...
2024: Case Reports in Dermatology
https://read.qxmd.com/read/38178864/real-life-experience-with-sonidegib-for-locally-advanced-basosquamous-carcinoma-a-case-series
#16
Enrico Bocchino, Simone Cappilli, Gerardo Palmisano, Andrea Paradisi, Alfredo Piccerillo, Alessandro Di Stefani, Ketty Peris
INTRODUCTION: Basosquamous carcinoma is an uncommon subtype of basal cell carcinoma (BCC), characterized by aggressive local growth and metastatic potential, that mainly develops on the nose, perinasal area, and ears, representing 1.2-2.7% of all head-neck keratinocyte carcinomas. Although systemic therapy with hedgehog inhibitors (HHIs) represents the first-line medical treatment in advanced BCC, to date, no standard therapy for advanced basosquamous carcinoma has been established. Herein, we reported a case series of patients affected by locally advanced basosquamous carcinomas, who were treated with HHIs...
2024: Case Reports in Dermatology
https://read.qxmd.com/read/38054030/diagnosis-management-and-outcome-of-bart-s-syndrome-observed-in-a-sub-saharan-african-country-senegal-dakar-2-case-reports
#17
Mame Tènè Ndiaye Diop, Maïmouna Bassoum, Khadim Diop, Yaye Diood Dieng, Birame Seck, Fatou Diasse Fall, Charles Tchibinda Delicat, Alassane Ndiaye, Assane Diop, Maodo Ndiaye, Pape Moctar Faye, Moussa Diallo, Ousmane Ndiaye, Fatimata Ly, Suzanne Oumou Niang
INTRODUCTION: Bart's syndrome is an uncommon inherited congenital disorder associating congenital cutaneous aplasia of the extremities and inherited epidermolysis bullosa. Bilateral and symmetrical involvement of the limbs is exceptionally described on black skin. In most cases, the diagnosis is clinical; however, the management remains very difficult and the extended forms are a real therapeutic challenge. We report 2 cases of Bart's syndrome observed in a sub-Saharan African country (Senegal, Dakar)...
2023: Case Reports in Dermatology
https://read.qxmd.com/read/38023344/green-nail-syndrome-treated-with-ozenoxacin-two-case-reports
#18
Terenzio Cosio, Rosalba Petruccelli, Roberta Gaziano, Carla Fontana, Marco Favaro, Paola Zampini, Enrico Salvatore Pistoia, Laura Diluvio, Flavia Lozzi, Luca Bianchi, Elena Campione
Green nail syndrome (GNS) is a persistent greenish pigmentation of the nail plate, originally described in 1944 by Goldman and Fox, due to Pseudomonas aeruginosa infection. Recently, pulmonary co-infection of P. aeruginosa and Achromobacter spp. has been described in patients with cystic fibrosis. Achromobacter xylosoxidans is a multidrug-resistant (MDR) pathogen involved in lung and soft tissue skin infections. Both Achromobacter xylosoxidans and P. aeruginosa are mainly found in humid environments or in water...
2023: Case Reports in Dermatology
https://read.qxmd.com/read/37933229/a-case-of-lip-psoriasis-in-a-14-year-old-boy-successfully-treated-with-adalimumab
#19
Francesca Caroppo, Laura Gnesotto, Maria Ludovica Deotto, Roberto Salmaso, Anna Belloni Fortina
Psoriasis is a common chronic skin disease mainly located in areas of friction. Psoriasis of the lips as an exclusive presentation is rare and often misdiagnosed. Different anti-psoriatic therapies have been proposed, but the literature is limited to case studies with partial results. Biologic therapies have revolutionized the management of many dermatologic conditions, including psoriasis, and they are approved for pediatric use. We report the case of a 14-year-old boy with a 2-year history of white-yellowish scaling lesions on his lips, without intraoral involvement...
2023: Case Reports in Dermatology
https://read.qxmd.com/read/37933228/bullous-lichen-planus-of-the-nails-a-case-report-and-review-of-the-literature
#20
Jonathan K Hwang, Cynthia M Magro, Shari R Lipner
Lichen planus is a chronic inflammatory disorder that may affect the skin, nails, and/or oral mucosa. Bullous lichen planus is a rare variant of lichen planus, which is even less common in the nails. We present a case of nail bullous lichen planus, in a 48-year-old male presenting with a 10-month history of onychodystrophy of all ten fingernails. A longitudinal excision of the left thumbnail was performed, with histopathology consistent with lichen planus with focal transition to bullous lichen planus. He was treated with intralesional triamcinolone injections to the fingernails monthly, with improvements noted after three treatments...
2023: Case Reports in Dermatology
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