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In the context of the child's nephrotic status and focal neurological signs, we had a high suspicion of cerebral venous thrombosis, and made a presumptive diagnosis.
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The child was started on high dose subcutaneous unfractionated heparin daily.
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This decision was made cautiously, but it was felt that the advantages surpassed the risks.
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He also received dexamethasone, high flow oxygen, and elevation of the head to 45 degrees, in order to treat features of raised intracranial pressure.
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On day 6 of admission his headache had improved and his focal neurological signs began to resolve.
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He still had a partial right VI nerve palsy and a convergent squint.
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His oedema resolved completely by day 10 of treatment, and he was discharged on day 18.
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He continued prednisolone 60mg daily for a total of 6 weeks, followed by a reduced dose of 40mg on alternate days for 6 weeks.
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At 12 weeks follow-up, his urinalysis showed a trace proteinurea but he remained in remission.
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A 43-year-old non-diabetic Indian male reported to our outpatient department with chief complaints of cough with expectoration, chest pain, reduced appetite, fever with chills, and night sweats for two weeks.
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He also complained of breathlessness on exertion and had two episodes of blood in his sputum.
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The patient explained that the cough was continuous and was relieved after taking cough syrup.
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He also mentioned that the episodes of fever were initially intermittent and then daily for the last two weeks and were relieved after taking Paracetamol.
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The chest pain was localized to the middle of the chest and was aggravated on exertion.
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He was a businessman by profession with no history of smoking, alcoholism, or any other substance abuse.
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Also, there was no history of any contact of TB or COVID-19 in the family or close contacts.
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And there was no history of foreign travel in the recent past.
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But he had reported having traveled by a domestic airline about twenty days back.
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There was no history of weight loss or any other major illness in the past.
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On examination his vitals were-pulse-108/minute, arterial BP-130/80 mm of Hg, respiratory rate of 30 breaths/minute, Sp02-899% on room air, temperature- 101-degree centigrade.
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His Sp02 fell by 70% on room air after waking.
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On auscultation, there was crepitation on the bilateral middle lobes of the lungs.
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Also, dyspnea on exertion was noted.
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The rest of the systemic examination was within normal limits.
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Considering this as a probable case of TB with COVID-19 he was advised a chest radiograph with sputum microscopy (Ziehl Neelsen (ZN) staining for acid-fast bacilli), Cartridge-based nucleic acid amplification test (CBNAAT) of the sputum and other routine investigations.
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To check for the COVID-19 he was advised qualitative polymerase chain reaction (PCR) test from the oropharyngeal swab.
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The results were surprising with Mycobacterium tuberculosis detected on sputum fluorescent microscopy and were also confirmed by the CBNAAT.
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However, there was no resistance to Rifampicin.
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The results of the PCR were positive for RNA specific to SARS-CoV-2.
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Besides, the chest radiograph PA-view was suggestive of bilateral consolidations on the middle lobes of lungs with ill-defined borders.
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The other investigations revealed a low lymphocyte count (1x 10 9 /L) and increased levels of C-reactive protein (CRP) (57 mg/L), lactate dehydrogenase (LDH) (580 U/L), and erythrocyte sedimentation rate (ESR) (70 mm in the 1 st hour).
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Also, a sample for liquid culture (MGIT BACTEC) was sent to the Intermediate Reference Laboratory (IRL) which revealed the growth of Mycobacterium tuberculosis.
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Computed tomography was not performed as the diagnosis was established by other cheaper and faster methods and also the patient was unwilling for the same.
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All the other routine investigations were within normal limits.
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He was referred to the nearest designated COVID-19 management center, where he was managed as per national guidelines.
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Besides, he was also started on an antitubercular treatment of four drugs as per the National Tuberculosis Elimination Program (NTEP) guidelines.
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He was advised follow-up post completion of his stay at the designated COVID-19 center, but he has not yet reported back for follow-up.
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Written informed consent was obtained from the patient for using clinical data and images for publication in this study.
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We report a case of a male near-term neonate with gestational age of 35 weeks.
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[ 2, 1, 0, 0, 0, 2, 7, 7, 7, 7, 7, 7, 7, 7, 7, 7, 0 ]
He was the third born child to a 27-year-old mother with no significant past history.
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[ 2, 0, 0, 0, 0, 1, 0, 2, 7, 7, 7, 7, 0, 0, 0, 0, 1, 0 ]
He was derived from a third degree consanguineous marriage.
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[ 2, 0, 1, 0, 0, 0, 0, 0, 1, 0 ]
He was born by means of normal vaginal delivery with a normal extra-uterine adaptation.
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[ 2, 0, 1, 0, 0, 0, 0, 0, 1, 0, 0, 0, 0, 0, 1, 0 ]
Meconium-stained amniotic fluid was noted.
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[ "CUI_LESS", "CUI_LESS", "CUI_LESS", "CUI_LESS", "CUI_LESS", "CUI_LESS", "CUI_LESS" ]
[ 3, 8, 8, 8, 0, 1, 0 ]
His birth weight was 3030g (75 th Percentile).
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[ 0, 0, 1, 0, 5, 0, 0, 0, 0, 0, 0 ]
The baby had normal physical examination at birth aside transitory respiratory distress.
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[ 2, 7, 0, 0, 0, 1, 0, 1, 0, 0, 0, 1, 0 ]
He had been hospitalized for four days in a private clinic, for the suspicion of materno-foetal infection, where he had antibiotics for 48 hours.
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He had developed no symptoms during his hospitalization.
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The output's weight was 2400g which signify the loss of 630g.
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[ 0, 0, 0, 1, 0, 5, 0, 0, 0, 1, 0, 0, 0 ]
Back home, he received exclusive maternal breastfeeding.
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On his fifth day of life, he presented multiple yellowish-watery stools (ab 12 times) and refuse feeding with apyrexia context.
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He had clinical signs of severe dehydration without fever or vomiting.
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He lost 930g relative to the birth's weight.
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The abdomen appeared neither tender nor distended, and the rest of his physical examination was normal.
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The laboratory findings revealed hypernatremia of 152mEq/L, hyperkalemia of 7,8mEq/L and severe metabolic acidosis: blood PH: 7,1, HCO3:4mEq/L.
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The osmotic gap was 45.
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There was no leukocytosis, and the serum level of C-reactive protein was normal.
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The infant was treated with intravenous fluids and electrolytes as well as antibiotics after obtaining blood and stool cultures, assuming an infectious etiology.
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After 26 hours of rehydration therapy, the dehydration resolved, however, a functional acute renal failure complicated by acidosis and hyperkalemia appeared.
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The chest radiograph showed "bat wings" pattern and the cardiothoracic index was 0, 45.
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The renal ultrasound showed discretely hyperechoic kidneys cortex and the absence of renal malformations.
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On the 11 th day of life, he was transferred to the pediatric intensive care unit.
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He needed mechanical ventilation for three days and exclusive parenteral feeding by central catheter.
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The evolution was burdened by cholestasis due to the prolonged parenteral feeding and nosocomial infection by staphylococcus epidermidis.
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Since his admission, he had developed a slimy diarrhea with 3 to 4 stools per day.
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He presented a profuse diarrhea during each attempt to introduce enteral feeding by hydrolyzed milk formula.
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He was discharged after 32 days with output's weight 3250g.
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The oesophago-gastro-duodenoscopy and duodenal biopsy showed partial villous atrophy associated to the brush border abnormalities.
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The periodic acid Schiff (PAS) stain revealed abnormalities in the brush border characterized by loss of the linear part of enterocytes with the presence of intra-cytoplasmic PAS + band in the apical pole of enterocytes uneven thickness and sometimes with double contours pattern.
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In the submucosa, there were numerous Brunner glands.
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We find the existence of numerous hemorrhagic suffusions.
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The CD10 immunostain was positive.
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Thus, a diagnosis hypothesis of MVID was raised.
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The electron microscopic examination confirmed the diagnosis.
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Mutation analysis of peripheral blood samples of the neonate revealed a mutation at the homozygous status of MYO5B gene.
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The baby died, after 97 days of life, of septic shock and multiple organ failure.
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A 20 years old man presented with fever, myalgias, arthralgias, retro-orbital pain, vomiting and gum bleeding during a large dengue outbreak in Lahore, Pakistan.
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On 7th day of illness patient became afebrile, but he developed severe headaches, unconsciousness followed by altered behavior.
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On 9th day of illness patient developed painful neck swelling accompanied by fever, tremors, palpitations, hoarseness of voice and odynophagia.
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Examination revealed acutely swollen, tender thyroid gland along with features of hyperthyroidism.
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Laboratory evaluation revealed stable hematocrit, thrombocytopenia and leukopenia.
[ "Laboratory", "evaluation", "revealed", "stable", "hematocrit", ",", "thrombocytopenia", "and", "leukopenia", "." ]
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Patient had seroconverted for anti-dengue IgM antibodies on the 10th day of illness.
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A non-contrast Computed Tomogram (CT) of the brain showed right frontal lobe hematoma.
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Thyroid profile showed increased free T3 and T4 and low TSH.
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Technetium thyroid scan showed reduced tracer uptake.
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He was diagnosed as having subacute thyroiditis and treated with oral prednisolone and propranolol.
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Follow up CT brain showed resolving hematoma.
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Patient's recovery was uneventful.
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A 17 year-old woman with a history of moderate persistent allergic asthma has benefited from a first desensitization protocol at age 3.
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The protocol has been interrupted 4 years later because of a mild skin reaction.
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Her doctor decided to stop the specific immunotherapy.
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But another doctor restarted a new protocol of desensitization at age 16 against pollens because of a lack of control of his condition.
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She was never hospitalized, she was receiving no medication and she was doing well one year after she received a new regimen of pneumallergens (Alustal® Stallergenes SA, France).
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Indeed, 12 hours after initiation of treatment, she complained of abdominal pain, vomiting and diarrhea without fever.
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Several hours after, she consulted to the emergency department where a surgical emergency was ruled out.
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She was then admitted to the internal medicine ward.
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Two days later, she developed an acute respiratory failure and was referred to the intensive care unit where laboratory tests revealed multiorgan failure: liver enzymes, 5000U/L (normal level, 0-37U/L); creatine phosphokinase, 59000U/L (normal level, 10-200U/L); cardiac troponin T, 21ng/ml (normal level, under 0,01ng/ml); leucopenia, 2600/mm 3 (normal level, 4000-9000/ mm 3); thrombocytopenia, 13000/ mm 3 (normal level, 150000-400000/ mm 3); prothrombin time, 38% (normal level, 70-100%).
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Chest X-ray demonstrated bilateral interstitial markings with a normal cardiac silhouette.
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Viral serology was normal for hepatitis A, B, C, D, and E, Epstein-Barr virus and Cytomegalovirus.
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A skin morbilliform rash and facial edema appeared later.
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[ "CUI_LESS", "C0234918", "C0234918", "C0234918", "CUI_LESS", "C0542571", "C0542571", "CUI_LESS", "CUI_LESS", "CUI_LESS" ]
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The patient received a fluid resuscitation, platelet and erythrocyte transfusion, steroids and antibiotics.
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[ "CUI_LESS", "CUI_LESS", "CUI_LESS", "CUI_LESS", "CUI_LESS", "CUI_LESS", "CUI_LESS", "CUI_LESS", "CUI_LESS", "CUI_LESS", "CUI_LESS", "CUI_LESS", "CUI_LESS", "CUI_LESS", "CUI_LESS", "CUI_LESS" ]
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