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We present the case of a nine-month-old male child with three days of fever, irritability, left focal seizure, and febrile focal status epilepticus. He had no history of previous comorbidities. A lumbar puncture was performed, which showed cerebrospinal fluid (CSF) leukocytosis; protein and glucose were normal, and the polymerase chain reaction (PCR) panel for 14 pathogens in CSF was negative. Immunoglobulin G (IgG) qualitative and quantitative tests were positive for coronavirus disease 2019 (COVID-19) upon arrival. An MRI performed one week after the initial onset showed findings suggestive of acute necrotizing encephalopathy (ANE). The patient required mechanical ventilation. However, his symptoms did not improve and follow-up imaging two weeks later showed progression of the disease with hemorrhagic changes. To our knowledge, this is the first reported case of ANE associated with severe acute respiratory syndrome coronavirus 2 (SARS-CoV-​2) infection in a pediatric patient

La epilepsia es la principal causa de consulta neurológica en niños peruanos. Sin embargo, hay escasa información sobre sus características clínicas y epidemiológicas. Objetivos: Presentar las características clínicas de los niños epilépticos atendidos en el Hospital Cayetano Heredia, entre los años 2010 y 2016. Material y métodos: Se realizó un estudio observacional descriptivo, retrospectivo, tipo serie de casos, basado en las historias clìnicas de en niños menores de 14 años con diagnóstico de epilepsia, seguimiento clínico, registro electroencefalogràfico y neuroimagenes. Resultados: Se incluyeron 193 pacientes. El 47,2% (91/193) presentaron su primera crisis epiléptica antes del año de edad, cuya etiología fue secundaria en el 59,3% (54/91), destacando los factores perinatales y las malformaciones cerebrales. La etiología primaria fue más frecuente en los niños que iniciaron las crisis después del año de edad. Las crisis generalizadas se presentaron en 64,2% (124/193) sin diferencias por grupos etarios. El 69,9% (135/193) fueron controlados con un solo fármaco, en tanto que el 15% (29/193) fueron refractarios al tratamiento. La comorbilidad ocurrió en el 68,4% (132/193), siendo frecuentes el retraso del desarrollo psicomotor, el retardo mental y la parálisis cerebral. Conclusiones: La mayoría de los niños presentaron su primera crisis antes del año de edad, generalmente de causa secundaria. En los niños mayores fue prevalente la etiología primaria. La mayoría fueron controlados con monoterapia, pero se registró un porcentaje de refractariedad al tratamiento. La comorbilidad fue muy frecuente.

Acute liver failure is the development of severe hepatic injury with deterioration of liver synthesis function and encephalopathy. Among all the variety of causes, neoplastic infiltration represents less than 0.5%. We present the case of a male patient with a past medical history of HTLV-1 infection, who reports symptoms of acute hepatitis, being diagnosed with Adult T-cell leukemia/lymphoma. Unfortunately, the patient had a rapid deterioration and passed away a few days after admission.

Infection by the Human T- Lymphotropic virus I (HTLV-1) causes Adult T cell Leukemia-lymphoma (ATLL), being the duodenal involvement rare. Commonly, patients co-infected with HTLV-1 and Strongyloides stercoralis are seen due to the lack of TH2 response found on these patients. We describe a 48-year- old woman, from the jungle of Peru, with a family history of HTLV-1 infection, who presented with a History of chronic diarrhea and weight loss. HTLV-1 infection with ATLL and strongyloidiasis were diagnosed. Ivermectin treatment and chemotherapy were initiated, being stabilized, and discharged. We report this case because of the unusual coexistence in the duodenum of ATLL and strongyloidiasis.

We present the case of a 30-year old female with a history of abdominal pain, fever, poor oral tolerance and weight loss for 6 months. An abdominal CT scan showed marked gastric dilatation due to extrinsic compression from lymphadenopathies around the second portion of the duodenum. The upper endoscopy revealed the presence of a penetrating gastric ulcer in the greater curvature. Biopsies of the lesions showed hystiocytes with granulomatous features and Acid Fast Bacilli (AFB) positive, and the cultures grew Mycobacterium tuberculosis sensitive to Isonazid and Rifampin. Subsequently anti-TB regimen was initiated achieving great clinical and endoscopic improvement.

Liver involvement is usually seen in patients infected with the human immunodeficiency virus (HIV), especially in patients coinfected with hepatitis B or C, in alcohol abuse, etc. However, there is a group of patients who develop liver involvement and portal hypertension of unspecified cause. Non-cirrhotic portal hypertension (NCPH) is a liver disorder recently described, but potentially serious. It has been reported in HIV-infected patients with highly active antiretroviral therapy (HAART), specifically didanosine (DDI). The pathophysiology involves the infectious agent (HIV) and its treatment (HAART), since both generate a pre-hepatic portal venulopathy. Similarly, HIV infection produces a prothrombotic state by protein S deficiency leading to the obliteration of small hepatic venules. It has been postulated that DDI as a cofactor in the pathogenesis of NCPH. All this leads that many of the liver biopsies show nodular regenerative hyperplasia. We present the case of a HIV-infected patient who was treated with a longstanding DDI. She developed upper gastrointestinal bleeding (UGB) and ascites due to NCPH, whose diagnosis was confirmed by biopsy. However, there is no similar study in our country.

Chronic actinic enteritis is a malfunction of the small bowel, occurring in the 6 months post-radiotherapy, and it can be manifestated as malabsortion, stenosis, fistula formation, local abscesses, perforation and bleeding, We report a case of an elderly patient who presents an episode of obscure gastrointestinal bleeding (OGIB) secondary to actinic enteritis. She is a 64-year- old female patient with the past medical history of cervical cancer who received radiotherapy and brachytherapy. One year after the treatment, the patient presents a chronic episode of melena and symptomatic anemia and 1 week before the admission she had hematochezia. At admission she has hemodynamic instability with a hemoglobin value of 2.7 gr/dl. We did an upper endoscopy, a colonoscopy and abdomino-pelvic tomography without any findings of the bleeding’s source. Reason why an endoscopic capsule was done, showing bleeding areas in the medial and distal small bowel. The patient had another gastrointestinal bleeding requiring a surgery where they decide to do a resection of the small bowel and a right hemicholectomy. The pathology was compatible with actinic enteritis. The patient after the surgery had a torpid evolution, and finally dies. We describe this case and do a review of all the existent data around the world, because is the first case reported in Peru of an actinic enteritis as a cause of OGIB.

We report the first case of colitis due to Mycobacterium avium in a Peruvian patient with HIV/AIDS.

Hepatic Angiosarcoma is an uncommon neoplasia with an incidence between 0.5 to 2 % of primary hepatic tumors. Due to a nonspecific presentation it is very difficult to reach the diagnosis which is usually late and by that time the organ has been involved by tumor and surgical treatment is not possible. Because of CT limitations for staging and metastasis diagnosis, laparoscopy is used because it gives us better vision of the abdominal cavity and reliable information about tumor staging and prognosis. Final diagnosis is pathological and require inmunohistochemical confirmation with CD-31 and CD-34. Chemotherapy and radiotherapy have not demonstrated an improvement in the survival rate which is 6 months without treatment since diagnosis.We present a case of a 41 yo male patient without significant history with 2 months of nonspecific symptoms related to an hepatic tumor and ascites.

Se reporta el caso de un niño de 10 años que se presentó con dos semanas de enfermedad caracterizada por cefalea, vómitos, marcha tambaleante y somnolencia. El examen clínico reveló bradilalia, ataxia, hiperreflexia, nistagmo horizontal y vertical, parálisis del VI nervio craneal izquierdo y signos de frontalización. En la tomografía yresonancia cerebrales se encontró hidrocefalia obstructiva por un tumor de la fosa posterior. La anatomía patológica reveló Astrocitoma Pilocítico grado I (WHO).