Intranodal Hemangioma as a Differential Diagnosis of Melanoma Metastasis: A Case Report of a Rare Entity [0.03%]
罕见疾病案例报告：与黑色素瘤转移鉴别诊断的淋巴结内血管瘤病例报告
Nika Filipović,Klara Gaćina,Majda Vučić et al.
Nika Filipović et al.
Dear editor, Haemangiomas are common benign vascular tumours usually detected on skin, mucosal surfaces, and soft tissues. In some extremely rare cases, haemangiomas can occur within a lymph node and as such are classified as primary benign...
Case Reports
Acta dermatovenerologica Croatica : ADC. 2025 Dec;33(4):193-195. DOI: 2025
Lilly Esquivel-Pedraza,Silvia Méndez-Flores
Lilly Esquivel-Pedraza
A 30-year-old man with recent diagnosis of HIV-infection was seen in the hospital, because of a 1-month history of swollen lips, painful oral mucosa ulcers, cervical lymph nodes and skin lesions. The medical history showed a previous patien...
Case Reports
Acta dermatovenerologica Croatica : ADC. 2025 Dec;33(4):191-192. DOI: 2025
Unusual Case of Granulomatosis with Polyangiitis Complicated with Hormographilella aspergillata Skin Infection [0.03%]
一种罕见的肉芽肿性多血管炎并发粗糙枝孢霉皮肤感染病例报告
Suzana Ljubojević Hadžavdić,Kristina Galešić,Marta Prtajin Perica et al.
Suzana Ljubojević Hadžavdić et al.
Granulomatosis with polyangiitis (GPA) is a rare ANCA-associated small-vessel vasculitis that predominantly affects the respiratory tract and kidneys, while cutaneous manifestations occur less frequently. Opportunistic fungal infections com...
Case Reports
Acta dermatovenerologica Croatica : ADC. 2025 Dec;33(4):188-190. DOI: 2025
Nicolas Kluger,Lidiya Todorova
Nicolas Kluger
Dear Editor, Tattooing is a popular decorative procedure worldwide1,2. Its prevalence in adults ranges from 20 to 30%1,3. However, Google Trends (GT) infodemiological data indicate that interest in tattoos began declining before the COVID-1...
A case of Schöpf-Schulz-Passarge syndrome presented with widespread apocrine hidrocystomas showing variable clinical features [0.03%]
一例Schöpf-Schulz-Passarge综合征患者广泛出现顶泌汗腺水疱样囊肿并表现出不同的临床特征
Can Baykal,Süleyman Hilmi Duymaz,Alper Gezdirici et al.
Can Baykal et al.
Dear Editor, Genodermatoses are usually diagnosed in early childhood but diagnosis may be delayed in rare cases. Schöpf-Schulz-Passarge syndrome (SSPS) first described in 1971 is a rare type of autosomal recessive ectodermal dysplasia char...
Case Reports
Acta dermatovenerologica Croatica : ADC. 2025 Dec;33(4):182-184. DOI: 2025
Comprehensive Case Report on Folliculitis Decalvans in a Pediatric Patient [0.03%]
儿童雄激素性脱发患者秃发性毛囊炎综合病例报告
Dimitrios Motsios,Kalliopi Sotiropoulou,Sylvana Karabarba et al.
Dimitrios Motsios et al.
Folliculitis decalvans, typically observed in adult males, is rare in pediatric populations. This case report explores the diagnosis and management of a 12-year-old boy with this condition, marking a rare pediatric case in Greece. The patie...
Case Reports
Acta dermatovenerologica Croatica : ADC. 2025 Dec;33(4):178-181. DOI: 2025
Traumatic Ulcerative Granuloma with Stromal Eosinophilia of the Tongue: Mandatory Biopsy for a Great Clinical and Dermatoscopic Simulator [0.03%]
舌部创伤性溃疡性肉芽肿伴间质嗜酸性粒细胞增多：一种临床及皮肤镜下高度模拟疾病的必需活检诊断
Andrija Jović,Aleksandar Popović,Ivana Jocić et al.
Andrija Jović et al.
Fast-growing ulcerations in the oral cavity are clinically challenging lesions with potentially different pathogenesis. Traumatic ulcerative granuloma with stromal eosinophilia represents a benign oral mucosa lesion with unclear pathogenesi...
Case Reports
Acta dermatovenerologica Croatica : ADC. 2025 Dec;33(4):174-177. DOI: 2025
Atypical Presentation of Sweet's Syndrome: A Case Report and Review of the Literature [0.03%]
关于Sweet综合征一例不典型病例的报告及文献复习
Dajana Smoljan Filipović,Mislav Mokos,Ivan Franin et al.
Dajana Smoljan Filipović et al.
Sweet's syndrome (acute febrile neutrophilic dermatosis) is an inflammatory condition characterized by the abrupt onset of erythematous, oedematous plaques or nodules and a dense neutrophilic dermal infiltrate. Although usually associated w...
Milijana Relić,Snežana Relić,Nenad Relić et al.
Milijana Relić et al.
Aquagenic keratoderma (AK) is a rare acquired and transient disorder of stil unknown etiology. This keratoderma is characterized by the appearance of whitish or translucent papules and folds on the skin of the palms and soles, after contact...
The Impact of BRAF Mutational Status on Survival in Melanoma Patients: Single Centre Experience [0.03%]
BRAF基因突变状态对 melanoma患者生存影响的单中心体会
Leo Kovač,Gordana Žauhar,Damir Vučinić et al.
Leo Kovač et al.
Melanoma accounts for less than 2% of all cancers worldwide but is responsible for 80% of skin cancer-related deaths. Among the various genetic alterations in melanoma, BRAF and NRAS mutations are the most common. While multiple studies hav...