Archivos de Patologia https://reunido.uniovi.es/index.php/AP <p>La revista <strong>Archivos de Patología</strong> tiene como su <em>leiv motiv</em> difundir un enfoque multidisciplinario de la Disciplina Patológica, enfatizando su importancia en la práctica clínica diaria. <strong>Archivos de Patología</strong> se centra en el análisis de casos clínicos reales, sin dejar de lado tanto los temas doctrinales como las revisiones y actualizaciones en Patología. Todas ellas son potentes herramientas para fomentar la calidad de los conocimientos y la excelencia tan demandados por la sociedad médica en general.</p> Universidad de Oviedo es-ES Archivos de Patologia 2660-7611 ATYPICAL EPIDIDYMO-ORCHITIS WITH SCROTAL MANIFESTATION OF ENTAMOEBA HISTOLYTICA WITH CONCURRENT MORGANELLA MORGANII INFECTION. https://reunido.uniovi.es/index.php/AP/article/view/22230 <p>Epididymo-orchitis is a common cause of acute scrotal pain, typically resulting from bacterial infections, with approximately 600,000 cases diagnosed annually in the United States. While most cases are attributed to sexually transmitted pathogens such as Neisseria gonorrhoeae or Chlamydia trachomatis in younger men and gram-negative organisms like Escherichia coli in older patients, rare parasitic infections can complicate the clinical picture. We present the case of an 82-year-old male with a complex medical history, including severe coronary artery disease, hypertension, and a recent Transcatheter Aortic Valve Implantation (TAVI), who developed left-sided scrotal pain and swelling. Initially diagnosed with orchiepididymitis and treated with antibiotics, his condition deteriorated, leading to recurrent febrile episodes and worsening symptoms. Imaging revealed a multiseptated scrotal collection and ischemic testicular changes. Surgical exploration uncovered purulent material, which cultured Morganella morganii, and histopathological analysis surprisingly revealed Entamoeba histolytica morphology with phagocytosed erythrocytes, an exceedingly rare finding in extraintestinal amebiasis. Stool and serological tests for E. histolytica were negative, suggesting isolated scrotal involvement. The patient underwent left orchiectomy, received broad-spectrum antibiotics followed by targeted therapy, and recovered without recurrence over a five-month follow-up. <br>This case emphasizes the importance of considering rare parasitic infections in atypical or refractory presentations of epididymal-orchitis, particularly in regions where E. histolytica is endemic or in patients with unique clinical histories. The unusual scrotal involvement of E. histolytica, with only one other documented case, highlights the diagnostic challenges and emphasizes the role of a multidisciplinary approach combining surgical intervention, microbiological studies, and tailored antimicrobial therapy. This report expands the understanding of extraintestinal amebiasis and reinforces the need for vigilance in identifying rare etiologies in urological conditions.</p> Mario Paul Sánchez Pérez Patricia Castellanos Donoso Al Flores Bustamante Carlos Alberto Cárdenas Aguirre Severino Rey Nodar Derechos de autor 2025 Archivos de Patologia 2025-01-09 2025-01-09 4 3 18 30 10.17811/ap.v4i3.22230 GOOD SYNDROME PRESENTING WITH PROGRESSIVE MUSCLE WEAKNESS FOLLOWING THYMECTOMY https://reunido.uniovi.es/index.php/AP/article/view/22228 <p>We present the case of a patient with Good syndrome who developed progressive muscle weakness following thymectomy. Muscle biopsy revealed criteria consistent with inclusion body myositis. Throughout her illness, she developed pure red cell aplasia, respiratory failure, and recurrent respiratory infections. She was treated with intravenous immunoglobulins, pyridostigmine, and cyclosporine A, achieving stability in her hematologic condition but without improvement in her myopathic symptoms. This case highlights the potential role of the thymus in the pathogenesis of autoimmune manifestations.</p> Ricardo Gómez de la Torre María Folgueras Gómez Lourdes Sánchez Miranda Ariana Fonseca Mourelle Iván Fernández Vega Germán Moris de la Tassa Derechos de autor 2025 Archivos de Patologia 2025-01-09 2025-01-09 4 3 4 9 10.17811/ap.v4i3.22228 CARCINOMA EOSINOFÍLICO DE CÉLULAS RENALES SÓLIDO Y QUÍSTICO EN PACIENTE PEDIÁTRICO CON ESCLEROSIS TUBEROSA: REPORTE DE CASO. https://reunido.uniovi.es/index.php/AP/article/view/22229 <p>El carcinoma de células renales sólido y quístico, eosinofílico, es un subtipo raro de carcinoma renal de células claras, descrito desde 1976 e incluido en la última edición de la Clasificación de tumores urinarios y genitales de la OMS. Este carcinoma renal tiene una inmunohistoquímica característica CK20 positivo y CK7 negativo, su incidencia se desconoce y representa el 0.2% de todos los carcinomas renales de células claras. Su presentación suele ser indolente, pero existen registros de presentaciones más agresivas con enfermedad metastásica. Se reporta el caso de una paciente de 7 años con antecedentes de esclerosis tuberosa y lesión renal compleja de novo.</p> Alejandro Cardona Palacio Susana Rivera Cardona Alejandro Vélez Hoyos Sigifredo Ospina Ospina Derechos de autor 2025 Archivos de Patologia 2025-01-09 2025-01-09 4 3 10 17 10.17811/ap.v4i3.22229 DE LA VOCACIÓN AL RETIRO SILENCIOSO: “QUIET QUITTING” EN EL CONTEXTO DE LA PATOLOGÍA MÉDICA https://reunido.uniovi.es/index.php/AP/article/view/22225 <p>Sin resumen</p> Severino Rey Nodar Carlos Alberto Cárdenas Aguirre Derechos de autor 2025 Archivos de Patologia 2025-01-09 2025-01-09 4 3 1 3 10.17811/ap.v4i3.22225