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Then meropenem was switched to oral ciprofloxacin for another 4 weeks and the patient was discharged from the hospital, in full recovery.
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Follow-up sonogram obtained almost 2 months after the drainage showed completely normal liver parenchyma without any residual liver cavities.
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A 12-year-old girl was referred to Department of Oral Surgery, with a complaint of pain and swelling in the left of maxilla that appeared 3 months ago.
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The swelling was slowly progressive, associated with pain.
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However, the patient did not refer any motor or sensory deficit.
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There was no family history of similar swelling.
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Physical examination revealed a left maxillary swelling.
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There was no facial palsy.
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No cervical lymph node enlargement was seen.
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The oral examination showed a 4 cm x 5 cm, tender, compressible mass in the left maxilla, from the lateral incisor to the second premolar teeth.
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The tumor surface was smooth and red-purple.
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Several teeth were involved and displaced in the tumor mass.
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We noted the absence of canine.
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Vitality tests proved negative on the central and lateral incisor.
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Hight mobility of lateral incisor was noted.
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Orthopantomography and occlusal radiography showed a wide osteolytic area of the anterior left maxilla, extending from the first permanent molar to the central incisor.
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The canine was impacted.
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No root resorption was observed.
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The radiolucency was closely related to maxillary sinus and involving the nasal cavity.
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Haematological investigations showed normal serum calcium, phosphorus and parathormone (PTH) levels.
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The provisional diagnosis of benign tumor of the maxilla was made.
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The patient underwent excision and curettage of the mass with extraction of the canine and lateral incisor tooth.
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The wound was closed with interrupted sutures.
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The post-operative histopathological report revealed multinuclear giant cells scattered randomly throughout the cellular and fibrous vascular-rich tissue.
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New bone formation and granulation tissue rich in mononuclear inflammatory cells was revealed.
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The giant cells were multinucleated with bland-appearing nuclei, and the background stromal cells displayed no evidence of atypical mitoses.
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A diagnosis of giant cell tumor was established.
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During a 1-year serial clinical and radiological follow-up, there was no evidence of recurrence.
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The facial contour and masticatory function were well-preserved.
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A 16-year-old Indian boy presented to our hospital with a history of a lump in the lower back region since birth.
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Initially, it was small, but its size increased gradually over time to a size of 15 cm × 15 cm at presentation.
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There were no other associated abnormalities.
[ "There", "were", "no", "other", "associated", "abnormalities", "." ]
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Investigations revealed the lump to be a benign cystic teratoma.
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The patient underwent surgery, and the whole tumor, from its base to the vertebrae, was excised.
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Bisection of the tumor revealed that it contained hair and pultaceous material consistent with a teratoma, which was later confirmed by histopathologic examination.
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We observed a 29 y.o. female proband with the episode of venous thrombosis at the age of 18 and family history of thrombosis.
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The antithrombin level in our patient was low, 44-48% (AT deficiency type I).
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A new genetic variant c.662G > C (p.W221S) in the SERPINC1 gene was detected in proband and affected father but was absent in healthy sister.
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We used in silico tools to evaluate the possible impact of p.W221S variant on protein structure and function.
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In mutated SERPINC1 protein a new N-linked glycosylation site is formed, however, it is unclear if the glycosylation at 219-221 site is possible.
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An 80 year-old Caucasian male was diagnosed at an outside institution with Barrett's esophagus with high grade dysplasia and presented to our institution for therapy.
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The patient underwent endoscopic mucosal resection using a band ligation technique of an area of nodularity within the Barrett esophagus.
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Microscopic examination demonstrated extensive Barrett esophagus with high-grade dysplasia as well as a second tumor which was morphologically different from the surrounding high-grade dysplasia and which was positive for S-100, HMB 45 and Melan-A on immunohistochemistry, consistent with melanoma.
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Further workup of the patient demonstrated multiple radiologic lesions consistent with metastases.
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Molecular studies demonstrated that the melanoma was positive for the 1799T>A (V600E) mutation in the BRAF gene.
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The overall features of the tumor were most consistent with metastatic melanoma occurring in a background of Barrett esophagus with high-grade dysplasia.
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In May 2014 a 49 year gentleman was admitted for widespread mucocutaneous blistering diagnosed as PV by histology and immunofluorescence.
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After 6 weeks of treatment with systemic steroids and azathioprine the patient developed pulmonary emboli and started oral anticoagulation with warfarin.
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In late September, the patient re-presented with a severe flare of PV and a recurrent deep vein thrombosis despite oral anticoagulation within therapeutic range.
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Warfarin was changed to subcutaneous low molecular heparin in therapeutic dose while treatment for pemphigus was escalated: first azathioprine was switched to mycophenolate mofetil and the steroids dose increased; then due to poor response, intravenous immunoglobulins were given for three courses and finally he received four infusions of Rituximab that induced sustained remission.
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In April 2015 the dose of mycophenolate was decreased but anticoagulation was continued until the beginning of July 2015 to ensure that decreasing immune suppression did not allow the emergence of another flare with attendant thrombotic risk.
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A 62-year-old woman presented with complaints of epigastric pain and vomiting.
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Computed tomography showed a 27-mm, hyper-enhancing tumor in the prepyloric antrum.
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Upper endoscopy also showed a submucosal tumor causing subtotal obstruction of the gastric outlet.
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Because a gastrointestinal stromal tumor was suspected, distal gastrectomy was performed.
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Histopathological examination revealed spindle cell proliferation in the submucosal layer.
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The spindle cells had invaded the muscularis propria layer and extended to the subserosal layer.
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The tumor was finally diagnosed as an IFP based on immunohistochemical findings.
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No mutations were identified in the platelet-derived growth factor receptor alpha (PDGFRA) gene via molecular genetic analysis.
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A 22-year-old woman, without any formerly diagnosed diseases, presented to the emergency department with a 3 day history of dyspnea, fatigue and central chest pain.
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She reported increasing dyspnea that developed in the previous month.
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She also had intermittent pain in the small joints for several months.
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There was no family history of SLE.
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On examination, she had a temperature of 38.2°C, a heart rate of 115 beats/minute, blood pressure of 90/60mmHg, respiratory rate of 25 breaths/minute, muffled heart sounds and jugular distention.
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The electrocardiogram showed sinus tachycardia and low voltage.
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The chest radiograph showed an enlargement of the cardiac silhouette with a right-sided pulmonary effusion.
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The echocardiography revealed a large circumferential pericardial effusion, with diastolic collapse of the right atrium, dilated inferior vena cava and 30% respiratory variation of the Doppler mitral valve, confirming the diagnosis of cardiac tamponade.
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Initial workup showed normochromic normocytic anemia with hemoglobin at 8.5g/dl, CRP: 75mg/L, renal and liver function tests were normal.
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Emergency pericardiocentesis was indicated but could not be performed because of the incapability to place the guidewire into the pericardial cavity.
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So, urgent surgical pericardiectomy with window procedure was realized, 1200 of clear fluid was evacuated.
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The pericardial fluid contained 2900 white blood cells/mm³, 100 red blood cells/mm³, bacteriological culture and cytologic examinations yielded negative results.
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The pericardial biopsy showed features of nonspecific inflammation, malignancy and tuberculosis were ruled out.
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Further investigations were accomplished to determine the etiology.
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Immunological workup revealed antinuclear antibodies titer of 1:1280, positive anti-SSA and anti-SM antibodies and hypocomplementemia.
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The coombs test was positive.
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The diagnosis of systemic lupus erythematosus was established based on hemolytic anemia, serositis, arthralgia, positive anti nuclear and anti SM antibodies and low complement.
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The patient was started on intravenous therapy with methylprednisolone followed by prednisone 60mg by mouth daily with hydroxychloroquine.
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She had a good clinical response and control echocardiography showed complete resolution of the pericardial effusion without recurrence.
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A 36-year-old female showed mild swelling in the right upper eyelid.
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She lost her RGP contact lens seven months prior to her first visit, from trauma by her child's kick to the right eye.
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At the first examination, we felt a firm lump inferior to the right brow.
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Eversion of the upper eyelid also revealed a firm subconjunctival mass superior to the upper tarsus.
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After incising the conjunctiva, the RGP contact lens was found without a fibrous capsule and granulation tissue in the subconjunctival space.
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Three years after removal of the lens, the patient did not show any complications, including ptosis.
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A 14-year old boy with no significant past medical history presented to a small district hospital in southern Sierra Leone with a 4 day history of facial puffiness, peripheral pitting oedema, abdominal pains, and reduced urine output.
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On examination he was afebrile, BP150/110, heart rate 70.
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He had significant periorbital and facial oedema, pitting oedema from the feet to the knees, a distended abdomen, ascites, and tender hepatomegaly.
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Lab results showed haemoglobin 10.9 g/dl, packed cell volume 35%, and positive malaria parasites.
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Urea (14 mg/dl), creatinine (1.0 mg/dl), sodium (137 mmol/L), and potassium (3.7 mmol/L) were normal.
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Urinalysis, using a urine dipstick, revealed three pluses of proteinurea, which equates to ≥3g urinary protein per day.
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Lab facilities for the measurement of serum albumin were not available.
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The diagnosis of nephrotic syndrome was made and the patient was started on a course of prednisolone 60mg/day, Enalapril 2.5mg daily, anti-malarial treatment, and empirical broad spectrum IV antibiotics to cover bacterial infections, in addition to a salt-restricted diet.
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On day 3 of admission he showed a clinical response to treatment, as the facial oedema, ascites, and BP had reduced.
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Urinalysis showed two pluses of proteinurea (0.5-1.0 gram per day per day).
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The child complained of a moderate headache, but had no fever, meningism, or focal neurological signs.
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He was started on oral paracetamol.
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The next morning (day 4 of admission) his symptoms evolved: his headache became severe, he had pain behind both eyes, and he was vomiting.
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Examination showed a right VI nerve palsy, diplopia, and tinnitus in the right ear, with some hearing loss.
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He later became drowsy and had a generalised seizure.
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Diagnosis and commencement of treatment was delayed due to the absence of CT/MRI brain imaging facilities in the local district.
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