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1.
World J Hepatol ; 14(11): 1977-1984, 2022 Nov 27.
Artigo em Inglês | MEDLINE | ID: mdl-36483603

RESUMO

BACKGROUND: Hepatic infarctions (HI) are ischemic events of the liver in which a disruption in the blood flow to the hepatocytes leads to focal ischemia and necrosis. Most HI are due to occlusive events in the liver's blood vessels, but non-occlusive HI may occur. They are associated with disruption of microvasculature, such as in diabetic ketoacidosis. While HI usually presents as peripheral lesions with clear borders, irregular nodular lesions may occur, indistinguishable from liver neoplasms and presenting a diagnostic challenge. CASE SUMMARY: We report a case of multiple extensive HI in a patient with poorly controlled diabetes mellitus, who first presented to the emergency room with diabetic ketoacidosis. He then developed jaundice, thrombocytopenia, and a marked elevation of serum aminotransferases. An ultrasound of the liver showed the presence of multiple irregular lesions. Further investigation with a computerized tomography scan confirmed the presence of multiple hypoattenuating nodules with irregular borders and heterogeneous appearance. These lesions were considered highly suggestive of a primary neoplasm of the liver. While the patient was clinically stable, his bilirubin levels remained persistently elevated, and he underwent an ultrasound-guided percutaneous biopsy of the largest lesion. Biopsy results revealed extensive ischemic necrosis of hepatocytes, with no signs of associated malignancy. Three months after the symptoms, the patient showed great improvement in all clinical and laboratory parameters and extensive regression of the lesions on imaging exams. CONCLUSION: This case highlights that diabetic ketoacidosis can cause non-occlusive HI, possibly presenting as nodular lesions indistinguishable from neoplasms.

2.
Am J Case Rep ; 19: 438-441, 2018 Apr 13.
Artigo em Inglês | MEDLINE | ID: mdl-29650946

RESUMO

BACKGROUND Acute promyelocytic leukemia (APL) is a very rare leukemia in children. Extramedullary involvement by APL has been reported in between 3-5% of cases, mainly associated with cases of relapse. A rare case of relapse of APL in a 9-year-old child is presented with skin involvement with myeloid sarcoma. CASE REPORT A 9-year-old male child was admitted to the Oncology Service of the hospital complaining of fever, progressive fatigue, oral petechiae with severe bleeding in the oral cavity. Bone marrow examination showed some promyelocytes. Flow cytometry showed 86% immature myeloid cells with the t(15;17) translocation, and molecular analysis showed expression of the PML/RARa fusion protein, which confirmed the diagnosis of APL. The patient completed a course of daunorubicin, cytarabine, and AII trans-retinoic acid (ATRA) with complete remission. After six months, the patient was re-admitted to hospital with a violaceous lesion on the scalp, with relapse of APL. Histological and immunohistochemistry of the lesion involving the skin of the scalp showed a myeloid sarcoma invading the dermis. CONCLUSIONS Myeloid sarcoma, also called granulocytic sarcoma, is an extramedullary tumor of immature myeloid cells, which very rarely presents in children with APL. The mechanisms that lead to myeloid sarcoma in children with APL and the possible association with ATRA therapy remain to be investigated.


Assuntos
Leucemia Promielocítica Aguda/diagnóstico , Doenças Raras , Sarcoma Mieloide/diagnóstico , Couro Cabeludo , Neoplasias Cutâneas/diagnóstico , Biópsia , Criança , Evolução Fatal , Citometria de Fluxo , Humanos , Masculino , Células Mieloides/patologia
3.
Am J Case Rep ; 18: 692-695, 2017 Jun 21.
Artigo em Inglês | MEDLINE | ID: mdl-28635683

RESUMO

BACKGROUND Blastic plasmacytoid dendritic cell neoplasm (BPDCN) is a rare hematodermic malignancy neoplasm with highly aggressive course and poor prognosis. This disease typically presents with cutaneous involvement as the first manifestation, with subsequent or simultaneous spread to bone marrow and peripheral blood.  CASE REPORT Here, we report the case of a 51-year-old woman who presented a violaceus skin lesion on the lateral region of the right thigh, weight loss, fever, and lymphadenopathies. Computed tomography (CT) displayed thoracic and abdominal lymph node and alveolar bleeding. Flow cytometry from circulating blastic cells was compatible with BPDCN (CD4+, CD56+ and CD123+). She underwent 5 cycles of hyper-CVAD alternating with high-dose methotrexate and cytarabine, but the patient died due to alveolar bleeding and sepsis. CONCLUSIONS We report a rare case of BPDCN characterized by an aggressive course, presence of atypical skin lesion, a finding suggestive of pulmonary infiltration, and nonresponse to induction chemotherapy, leading to late diagnosis and therapeutic management. Because of the late recognition of the skin lesion, neoplastic cells infiltrated the dermis and spread as the disease progressed rapidly to a fatal course.


Assuntos
Células Dendríticas/patologia , Neoplasias Hematológicas/patologia , Neoplasias Pulmonares/patologia , Neoplasias Cutâneas/patologia , Evolução Fatal , Feminino , Humanos , Linfonodos/patologia , Pessoa de Meia-Idade
4.
Rev. Soc. Bras. Clín. Méd ; 16(3): 164-166, jul.-set. 2018. graf.
Artigo em Português | LILACS | ID: biblio-1047946

RESUMO

OBJETIVO: Caracterizar o perfil de mortalidade por câncer de cavidade oral. MÉTODOS: Estudo transversal, descritivo e retrospectivo construído por meio de dados obtidos na plataforma do Departamento de Informática do Sistema Único de Saúde (DATASUS) em um recorte de 5 anos (2012-2017). O nível de significância considerado foi de 5%. RESULTADOS: No período analisado, foram registradas 151.573 internações no Brasil por câncer de cavidade oral. Do total, 72,7% pertenciam ao sexo masculino. CONCLUSÃO: O conhecimento do perfil de mortalidade por câncer de cavidade oral permitiu refletir acerca do modelo de atenção por meio de uma abordagem sistematizada, com o intuito de gerar desfechos mais favoráveis na saúde pública. (AU)


OBJECTIVE: To characterize the oral cavity cancer mortality. METHODS: This is a cross-sectional, descriptive and retrospective study constructed using data obtained from the Brazilian Informatics Department of the National Unified System platform, analyzed in a 5-year cut (2012-2017). The level of significance considered was 5%. RESULTS: In the period analyzed, 151.573 hospitalizations were recorded in Brazil for oral cavity cancer. Of the total, 72.7% were male. CONCLUSION: The knowledge of the oral cavity cancer mortality profile allowed the reflection on the care model through a systematized approach, aiming to generate more favorable outcomes in public health. (AU)


Assuntos
Humanos , Masculino , Feminino , Pré-Escolar , Criança , Adolescente , Adulto , Pessoa de Meia-Idade , Idoso , Idoso de 80 Anos ou mais , Neoplasias Bucais/mortalidade , Brasil/epidemiologia , Neoplasias Bucais/epidemiologia , Estudos Transversais , Estudos Retrospectivos , Distribuição por Sexo , Distribuição por Idade , Hospitalização/estatística & dados numéricos
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