Volume 13 - Issue 1


Authors : K.V. Pikul, V.I. Ilchenko, O.V. Muravlova, Z.O. Shaienko, I.V. Dvornyk
The scale of the HIV/AIDS epidemic in Ukraine, as well as around the world, continues to grow. Today, complete healing from HIV infection, unfortunately, impossible. Our country is going through difficult times of upheaval, we have been struggling with coronavirus disease for 4 years, now there is martial law and associated with it consequences of blood transfusions, medical care, which can indirectly affect HIV infection in people.
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Authors : Ana Belén Gálvez Ruiz, M. Leonor Senent Peris, Rafael Andreu Lapiedra, Amparo Sempere Talens, Vicent Martínez Cózar, Carmen Rodríguez García, Ana Isabel Vicente Sáncez, María Dolores Linares Latorre, Juana Clavel Pia, Lourdes Cordón Gallego, Nuria Rausell Fontestad, Irene Luna del Valle
A 55-year-old woman presents to the Emergency Room with a 3-month history of right hemibody hypoesthesia and increasing difficulty performing activities of daily living. No fever was reported. Blood tests showed: lactate dehydrogenase (LDH) 310 U/L, C-reactive protein (CRP) 66.4 mg/L, hemoglobin 10.6 g/dL, mean corpuscular volume (MCV) 95 fL, white blood cell count (WBC) 11,93 x103/µL (neutrophils 9,04, lymphocytes 1,43, monocytes 1,300 x103/ µL), platelets 188 x103/µL. Coagulation tests and peripheral blood smear were normal. Brain MRI revealed multiple bilateral hyperintense T2/FLAIR lesions with patchy leptomeningeal enhancement (images 1a and 1b). Lumbar puncture was normal, with no atypical cells or microbiological isolates.
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Authors : Trevor Russo OMS-IV, B.S*, Collin Eckhauser OMS-IV, B.S, Ryan Prusko M.D, John Gusz M.D, David Hughes M.D, PhD
Jejunal diverticulosis is a rare condition that is oftentimes asymptomatic but can lead to serious complications such as perforation, hemorrhage, or obstruction. Due to its nonspecific presentation, perforated jejunal diverticulitis is frequently misdiagnosed, resulting in delayed management and increased morbidity.
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Authors : Ravi Shankar B, Shruti Sagar B, Rajasekhar Reddy, Naveen Chand Perugu, Janger Bee, Adepu Bhavani
Hepatobiliary tuberculosis is a rare manifestation of Mycobacterium tuberculosis infection and is usually secondary to tuberculosis of the lungs or gastrointestinal tract. Diagnosis is difficult in many situations because of its rarity and presentation in the form of non-specific symptoms and signs and lack of any defined criteria on imaging studies. Histopathological examination is necessary for definitive diagnosis. Recommended treatment is with conventional antituberculous drugs and surgical intervention is rare.
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Authors : M.Essouri*, S. Ben Ammar ,I.M. Abbassi, N.Toujani , Z. Teyeb N. Khammassi
This is the cerebral MRI of a 24-year-old patient with no notable medical history, referred by ophthalmologists for an etiological assessment of bilateral retrobulbar optic neuropathy. During the interview, the patient reported experiencing headaches and bilateral galactorrhea. Physical examination revealed no abnormalities.
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Authors : Yuliia Hurieieva; Jan Miksovsky*; Jan Lestak
The cohort consisted of two groups of patients with early stage POAG. Each group consisted of 10 people (20 eyes), 5 women and 5 men. The first group was treated with carteolol (carteol LP 2% eye drops) and the second with latanoprost (xalatan 0.005% eye drops). The duration of treatment was at least one year, Citicoline (NEUROTidine 50 mg/ml) was then added to both groups and taken for 4 months as an oral dose of 2x5 ml.
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