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La actinomicosis pélvica es una infección poco común del tracto genital inferior y la pelvis. La especie causal más frecuente es la bacteria Actinomyces israelii, y se debe sospechar en toda paciente que presente dolor crónico pélvico y hemorragia uterina. Aunque se manifiesta excepcionalmente en mujeres sin antecedentes de portar dispositivos intrauterinos, es importante considerarla como diagnóstico. Se presenta el caso clínico de una paciente de 12 años con hemorragia uterina anormal resistente al tratamiento, que requirió intervención quirúrgica, incluyendo biopsia endometrial. El diagnóstico resultante fue actinomicosis endometrial. Este caso aporta la actualización del conocimiento sobre esta rara enfermedad y su presentación poco frecuente en adolescentes(AU)

Pelvic actinomycosis is a rare infection of the lower genital tract and pelvis. The most common causative species is the bacterium Actinomyces israelii, and it should be suspected in any patient who presents with chronic pelvic pain and uterine bleeding. Although it occurs exceptionally in women without a history of carrying intrauterine devices, it is important to consider it as a diagnosis. It is presented the clinical case of a 12-year-old patient with abnormal uterine bleeding resistant to treatment, which required surgical intervention, including endometrial biopsy. The resulting diagnosis was endometrial actinomycosis. This case contributes to updating knowledge about this rare disease and its uncommon presentation in adolescents(AU)

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Actinomycosis is a rare infectious disease characterized by slowly progressive, chronic suppurative lesions, often mistaken for malignancies due to its ability to mimic them. It is caused by Actinomyces bacteria, which are part of the normal flora of the human oropharynx, gastrointestinal, and urogenital tracts. This case report describes a 51-year-old male with a history of mandibular rhabdomyosarcoma presenting with severe shoulder and hip pain, dysphagia, and headaches, initially suspected to be a cancer recurrence. However, after further investigation, including a PET-CT and tonsillectomy, the diagnosis of actinomycosis was confirmed through histopathological examination. The case highlights the diagnostic challenges of actinomycosis, especially in patients with complex clinical histories, emphasizing the importance of considering it as a differential diagnosis in similar presentations. The patient was treated with long-term antibiotic therapy, predominantly beta-lactams, demonstrating the necessity of a comprehensive diagnostic approach and the implications of a delayed diagnosis. This case underscores the critical need for high clinical suspicion and awareness among healthcare professionals regarding the potential for actinomycosis to mimic more common diseases, ensuring timely and accurate treatment.

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Actinomycosis is an uncommon, subacute to chronic, suppurative bacterial infection caused by Actinomyces Israelii. About 3% of all actinomycosis cases occur in the tongue, often affecting adult patients (mean age, 50 years). The clinical characteristics of actinomycosis can resemble malignant or benign tumors, and other infectious diseases. A 56-year-old woman was referred presenting an ulcerated lesion on the tongue 1 year ago. Intraoral examination revealed an edematous nodular lesion with an ulcerated surface, slightly symptomatic, on the midline dorsum of posterior tongue, suggesting nodular median rhomboid glossitis. Cytology smear was negative for fungus. After excisional biopsy, histopathological examination showed a chronic inflammatory infiltrate supported by a fibrovascular connective tissue stroma, and at the deepest part, broad basophilic areas surrounded by neutrophils, containing numerous filamentous bacilli, which were highlighted by Gram and Groccott-Gomori staining. The final diagnosis was lingual actinomycosis. Oral amoxicillin treatment (8/8 h for 2 weeks) was started, and after 1-month complete resolution was observed. Lingual actinomycosis is a rare lesion that must be recognized by dentists, because its early diagnosis and correct treatment reduce the possibility of a clinical complication that compromises the patient's quality of life. Noteworthy, when located on the midline dorsum of posterior tongue, actinomycosis can simulate nodular median rhomboid glossitis, expanding its spectrum of clinical differential diagnosis.

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En la región cervicofacial los quistes de los maxilares de origen odontogénico constituyen una afección relativamente importante, los más frecuentes son los quistes radiculares. Se presentó un paciente masculino de 23 años de edad con un quiste radicular residual extenso que ocupaba la zona mandibular posterior izquierda, y acude a consulta estomatológica de la Clínica «Celia Sánchez Manduley» por un aumento de volumen que causa asimetría facial notable de la hemicara izquierda, de tres centímetros de diámetro, indoloro, asintomático, con 6 meses de evolución y consistencia dura; además refiere tratamiento de exodoncia de molar inferior en la zona (37) hace 2 años. Se indicó radiografía periapical y panorámica donde se observó zona radiolúcida bien definida de 35 a 38 con reabsorción de raíz mesial de 38, distal de 36 y movilidad dentaria grado II en ambos dientes. Se realizó exéresis de la lesión cuyo estudio histológico informó un quiste radicular residual.

Jaw cysts of odontogenic origin constitute a relatively important condition in the cervicofacial region, where radicular cysts are the most frequent. We present a 23-year-old male patient who come to "Celia Sánchez Manduley" Dental Clinic with an extensive residual radicular cyst that occupied his left posterior mandibular area and an increase in volume that caused him a notable facial asymmetry in the left side of his face, of three centimeters in diameter, painless, asymptomatic, with 6 months of evolution and hard consistency; he also mentions a lower molar extraction treatment in area (37) 2 years ago. Periapical and panoramic X-rays were indicated where a well-defined radiolucent zone of 35 to 38 was observed with mesial root resorption of 38, distal of 36 and grade II dental mobility in both teeth. Exeresis of the lesion was performed, whose histological study reported a residual radicular cyst.

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BACKGROUND: Actinomycosis is an unusual chronic bacterial infection, even rarer in people living with HIV. It is not considered an AIDS-defining disease. However, the role in co-presentation or overlap with other opportunistic conditions of advanced HIV is unknown. CASE PRESENTATION: A 49-year-old Peruvian male presented with a 4-month history of dysphagia, odynophagia, hyporexia and wasting. He underwent an upper digestive endoscopy, in which ulcers with a necrotic center were observed, therefore, the initial diagnostic assumption was esophageal cancer. Subsequent pathology report excluded neoplasms and confirmed the diagnosis of actinomycosis. Serology for human immunodeficiency virus was requested, yielding a positive result. Antimicrobial treatment with amoxicillin and antiretroviral therapy were indicated, with slow clinical improvement. After 4 months, epigastric discomfort presented, for which a new upper digestive endoscopy was performed, revealing a deep gastric ulcer, which was compatible with diffuse large B-cell non-Hodgkin lymphoma. CONCLUSION: Esophageal actinomycosis in people living with HIV is very rare. We suggest HIV-associated immunosuppression is not enough to allow for actinomycosis to develop, and masked underlying entities should be sought. The existence of such entities in people living with HIV should raise awareness of the possibility of unmasked immune reconstitution inflammatory syndrome once treatment has started.

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BACKGROUND: Allogeneic hematopoietic stem cell transplant (allo-HSCT) is used to treat several hematological diseases, but immunosuppression during allo-HSCT facilitates opportunistic microbial growth in tissues, such as actinomycosis. An effective diagnosis of opportunistic diseases is essential for correct management of the disease and preservation of the immunosuppressed patient's life. CASE DESCRIPTION: A 57-year-old female patient was diagnosed with extranodal nasal type NK/T cell lymphoma and underwent curative treatment with allo-HSCT. Twenty-one days after the last clinical follow-up, the patient presented a necrotizing lesion in the papilla region between the first and second molars of the second quadrant. Histopathological analysis showed the presence of a bacterial cluster consistent with Actinomyces infection, and a dense lymphoid infiltrate was also observed. Immunohistochemistry for CD20, CD3, and CD56 was performed to exclude the possibility of the recurrence of extranodal NK/T cell lymphoma. Oral microbiota profiling showed a huge increase in the abundance of Actinomyces bacteria in the subgingival region three weeks prior to appearance of the lesion. CONCLUSIONS: Opportunistic infections with an unusual clinical appearance are confounding factors in therapeutic decision-making. We present for the first time a case of actinomycosis in the gingival papilla region following allo-HSCT. We also highlight how microbiota profiling through next-generation sequencing could be used to anticipate bacterial infection diagnosis.

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ABSTRACT The aim of this study is to report an unusual case of actinomycosis in the maxilla region of an asymptomatic patient. A 21-year-old white man was referred for the analysis of panoramic radiography and cone beam computed tomography, where it was observed the presence of a hypodense lesion on the left side of the maxilla, which extended from the maxillary left central incisor to the region of the maxillary left second premolar. During intraoral examination, a depression was observed in the hard palate mucosa, as well as a fistula in the alveolar mucosa close to maxillary left central incisor, which had pulp vitality confirmed by thermal tests. A fistulography was performed, with periapical radiography, where it was found that the fistulous path did not originate from the tooth mentioned above. An incisional biopsy was performed for diagnostic purposes. However, given the inconclusive microscopic findings, four months later, a new biopsy was performed. The histopathological examination revealed the presence of a colony of microoganisms with filamentous pattern of radiated rosette, surrounded by polymorphonuclear inflammatory cells. Based on the morphological characteristics, the diagnosis of actinomycosis was established. The treatment was based on antibiotic therapy. Six months after treatment of the infection, no signs of recurrence were observed, and the patient remains in follow-up. Actinomycosis in the maxilla is an uncommon infection with a predilection for males between the ages of 20 and 60, whose treatment is antibiotic therapy associated or not with surgical excision.

RESUMO O objetivo deste estudo é relatar um caso incomum de actinomicose em região de maxila de um paciente assintomático. Um homem de 21 anos, branco, foi encaminhado para análise de radiografia panorâmica e tomografia computadorizada de feixe cônico, onde foi observada a presença de lesão hipodensa do lado esquerdo da maxila, que se estendia da região do incisivo central superior esquerdo ao segundo pré-molar superior esquerdo. Ao exame intrabucal, observou-se depressão na mucosa do palato duro, bem como fístula na mucosa alveolar próxima ao incisivo central superior esquerdo, no qual tinha vitalidade pulpar confirmada pelos testes térmicos. Uma fistulografia com radiografia periapical foi realizada, onde foi observado que o trajeto fistuloso não era originado do dente mencionado anteriormente. Foi realizada biópsia incisional para fins diagnósticos. Porém, diante dos achados microscópicos inconclusivos, quatro meses depois, uma nova biópsia foi realizada. O exame histopatológico revelou a presença de colônia de microrganismos com padrão filamentoso de roseta irradiada, circundado por células inflamatórias polimorfonucleares. Com base nas características morfológicas, foi estabelecido o diagnóstico de actinomicose. O tratamento foi baseado em antibioticoterapia. Seis meses após o tratamento da infecção, não foram observados sinais de recidiva e o paciente permanece em acompanhamento. A actinomicose da maxila é uma infecção incomum, com predileção por pacientes do sexo masculino com idade entre 20 e 60 anos, cujo tratamento é antibioticoterapia associada ou não à excisão cirúrgica.

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Introducción: La actinomicosis es una infección bacteriana supurativa crónica, producida por especies de Actinomyces, principalmente Actinomyces israelii. La localización en la pélvica es rara presentando el 3 % de toda la actinomicosis humana. Objetivo: Describir el caso clínico de una paciente que recibió tratamiento quirúrgico y se le diagnosticó actinomicosis pélvica sin asociación con el uso de dispositivos intrauterinos, lo que contribuye al conocimiento actual sobre una enfermedad poco frecuente. Caso clínico: Paciente femenina de 22 años de edad, color de la piel blanca, recibió tratamiento quirúrgico urgente por presentar como diagnóstico preoperatorio un absceso tubo-ovárico. Con la aplicación de anestesia general orotraqueal se realizó laparotomía exploradora, salpingooforectomía izquierda y lavado profuso de la cavidad abdominal sin complicaciones y se confirmó por el departamento de Anatomía Patológica el diagnóstico de actinomicosis pélvica. Cumplió tratamiento antimicrobiano por cuatro semanas y siete meses después de la intervención quirúrgica, se mantuvo asintomática. Conclusiones: La actinomicosis pélvica se debe sospechar en toda paciente con dolor crónico pelviano. Se manifiesta excepcionalmente en mujeres sin antecedente de ser portadoras de dispositivos intrauterinos. La presentación clínica es típicamente insidiosa por lo cual el diagnóstico con frecuencia se hace de forma tardía. Un alto índice de sospecha y una actitud diagnóstica activa son fundamentales para un tratamiento oportuno, seguro y eficaz.

Introduction: Actinomycosis is a chronic suppurative bacterial infection, produced by Actinomyces species, mainly Actinomyces israelii. Pelvic localization is extremely rare with 3% of all human actinomycosis. Objective: To describe the clinical case of a patient who received surgical treatment and was diagnosed with pelvic actinomycosis without association with the use of intrauterine devices, which contributes to current knowledge about a rare disease. Clinical case: A 22-year-old white female patient, received urgent surgical treatment for presenting as a preoperative diagnosis a tube-ovarian abscess. With the application of general orotracheal anesthesia, exploratory laparotomy, left salpingo oophorectomy and profuse washing of the abdominal cavity were performed without complications and the diagnosis of pelvic actinomycosis was confirmed by the Department of Pathological Anatomy. She completed antimicrobial treatment for four weeks and seven months after surgery, she remained asymptomatic. Conclusions: Pelvic actinomycosis is a disease that should be suspected in all patients with chronic pelvic pain, being an exceptional entity, in women with no history of being carriers of intrauterine devices. The clinical presentation is typically insidious so the diagnosis is often delayed. A high level of suspicion and an active diagnostic attitude are essential for timely, safe and effective treatment.

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A actinomicose é uma infecção rara causada por bactérias do gênero Actinomyces sp. que são importantes constituintes das flora comensal de animais e humanos, colonizando a orofaringe, o trato respiratório superior, o trato gastrointestinal e o trato genital feminino. Diante de uma lesão na mucosa associada a um desequilíbrio nas defesas do organismos, as bactérias se infiltram nas estruturas, gerando uma infecção. As áreas mais comumente afetadas por esta patologia correspondem às regiões cervicofacial (50%), abdominal (20%) e torácica (15 a 20%), sendo o envolvimento laríngeo bastante raro (< 5% dos casos), com poucos casos descritos na literatura. Este estudo visa relatar o caso de um paciente de 76 anos com actinomicose mimetizando neoplasia de laringe, através da revisão do prontuário, descrevendo o quadro clínico e evidenciando os exames de imagem realizados na investigação com o objetivo de alertar os profissionais de saúde e compartilhar informações sobre esta patologia para que possa fazer parte do diagnóstico diferencial de doenças granulomatosas e infecciosas da laringe, principalmente em pacientes com mais de 50 anos, visando o diagnóstico precoce e o tratamento adequado.

Actinomycosis is a rare infection caused by bacteria of the genus Actinomyces sp. which are important constituents of the commensal flora of animals and humans, colonizing the oropharynx, the upper respiratory tract, the gastrointestinal tract and the female genital tract. Faced with a lesion in the mucosa associated with an imbalance in the organism's defenses, the bacteria infiltrate the structures, generating an infection. The areas most commonly affected by this pathology correspond to the cervicofacial (50%), abdominal (20%) and thoracic (15 to 20%) regions, and laryngeal involvement is quite rare (< 5% of cases), with few cases described in the literature. This study aims to report the case of a 76-year-old patient with actinomycosis mimicking laryngeal neoplasm, through the medical record review, describing the clinical picture and evidencing the imaging tests performed in the investigation with the purpose of alerting health professionals and sharing information about this pathology so that it can be part of the differential diagnosis of granulomatous and infectious diseases of the larynx, especially in patients older than 50 years, aiming at early diagnosis and appropriate treatment.

La actinomicosis es una infección rara causada por bacterias del género Actinomyces sp. que son componentes importantes de la flora comensal de animales y humanos, colonizando la orofaringe, el tracto respiratorio superior, el tracto gastrointestinal y el tracto genital femenino. Ante una lesión de la mucosa asociada a un desequilibrio de las defensas del organismo, las bacterias se infiltran en las estructuras, generando una infección. Las áreas más comúnmente afectadas por esta patología corresponden a las regiones cervicofacial (50%), abdominal (20%) y torácica (15 a 20%), siendo la afectación laríngea bastante rara (< 5% de los casos), con pocos casos descritos en la literatura. El presente estudio tiene como objetivo relatar el caso de una paciente de 76 años con actinomicosis simulando neoplasia laríngea, a través de la revisión de la historia clínica, describiendo el cuadro clínico y mostrando los estudios de imagen realizados en la investigación, con el propósito de alertar a los profesionales de la salud y compartir información sobre esta patología para que forme parte del diagnóstico diferencial de las enfermedades granulomatosas e infecciosas de la laringe, particularmente en pacientes con edad superior a 50 años, con vistas al diagnóstico precoz y tratamiento adecuado.

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La persistencia de lesiones perirradiculares luego del tra- tamiento endodóntico es un problema que requiere del clínico un conocimiento cabal de la histofisiología y de la histopato- logía del sistema de conductos radiculares del tejido pulpar y de los tejidos perirradiculares (periodonto y hueso); además de considerar siempre la posible existencia de enfermedades sistémicas que también pueden actuar como factores de in- fluencia. La presencia de bacterias remanentes a posteriori del tratamiento es considerada como una de las causas principales y más frecuentes para la perpetuación de las lesiones perirra- diculares. Sin embargo, existen otros factores causales, como la existencia de conductos laterales o accesorios infectados y no tratados, la reabsorción dentinaria interna, intercomunica- ciones, cul-de-sacs o istmos; que representan áreas de difícil acceso durante la instrumentación e irrigación. Cuando la cau- sa original se localiza en la zona perirradicular, como en los casos de actinomicosis, reacciones a cuerpo extraño, cristales de colesterol (CRCo) y granulomas o quistes con alto conte- nido de CRCo, la indicación más adecuada es el retratamiento y la cirugía periapical como complemento (AU)

The persistence of periradicular lesions after endodontic treatment is a problem that requires the doctor to have a thor- ough knowledge of the histophysiology and histopathology of the root canal system, the pulp tissue and periradicular tis- sues (periodontium and bone); as well as always considering the possible existence of systemic alterations that can also be influencing factors. Persisting bacteria within the root canal system after treatment is one of the major and most frequent causes for the perpetuation of periradicular lesions. Howev- er, there are other possible causal factors such as the exist- ence of untreated lateral or accessory canals, internal dentin resorption, intercommunications, cul-de-sacs or isthmuses; areas that represent a difficulty in access during instrumen- tation and irrigation. If the original cause is located in the periradicular area, in cases like actinomycosis, foreign-body reactions, cholesterol crystals (CRCo) and granulomas or cysts with high content of CRCo, retreatment coupled with periapical surgery is the best approach to treatment (AU)

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