19/Jun/2019
Live fetus inside the urinary bladder: a case report
DOI: 10.31744/einstein_journal/2019RC4570
ABSTRACT Vesicouterine fistula is a rare condition. Its incidence, however, has been increasing due to the higher incidence of cesarean sections. The presence of a live fetus inside the bladder who passed through a vesicouterine fistula is an extremely rare situation. We report a case of woman who underwent two previous cesarean sections, was referred to a hospital due to mild pelvic pain and genital bleeding. At the moment, physical examination was normal. Ultrasound scan revealed a gestational sac inserted […]
Keywords: Abortion; Fetus; Obstetrics; Pregnancy; Pregnancy complications; Urinary fistula
08/Jun/2019
Treatment of ligneous conjunctivitis with heterologous serum
DOI: 10.31744/einstein_journal/2019RC4714
ABSTRACT Ligneous conjunctivitis is a rare form of chronic and recurrent bilateral conjunctivitis, in which thick membranes develop on the tarsal conjunctiva and on other mucosae. We report the case of a 55-year old female patient with bilateral ligneous conjunctivitis who was successfully treated with 50% heterologous serum. There was no recurrence or side effects after one-year follow-up. We suggest the use of 50% heterologous serum should be further studied to better determine its efficacy as a treatment option for […]
Keywords: Conjunctivitis/therapy; Plasminogen/deficiency; Serum
08/Jun/2019
Reproductive alternatives for patients with dystrophic epidermolysis bullosa
DOI: 10.31744/einstein_journal/2019RC4577
ABSTRACT Epidermolysis bullosa describes a group of skin conditions caused by mutations in genes encoding proteins related to dermal-epidermal adhesion. In the United States, 50 cases of epidermolysis bullosa per 1 million live births are estimated, 92% of which classified as simplex, 5% dystrophic, 1% junctional and 2% non-classified. Dystrophic epidermolysis bullosa is associated with autosomal, dominant and recessive inheritance. Epidermolysis bullosa causes severe psychological, economic and social impacts, and there is currently no curative therapy, only symptom control. Embryonic […]
Keywords: Basement membrane; Collagen type VII; Epidermolysis bullosa dystrophica; Genetic counseling; Heredity
13/May/2019
Left ventricular noncompaction in a Para athlete
DOI: 10.31744/einstein_journal/2019RC4514
ABSTRACT The left ventricular noncompaction is a congenital cardiomyopathy characterized by the presence of abnormal trabeculations in the left ventricle. The present study describes the case of a 14-year-old female Para athlete, who plays goalball. She was asymptomatic, with history of congenital nystagmus and mild visual impairment, who presented nonspecific electrocardiographic abnormalities during pre-competition screening. Cardiac magnetic resonance imaging showed left ventricular non-compaction (non-compacted to compacted layer ratio equal to 2.5) and mild biventricular systolic dysfunction. Initially, the patient was […]
Keywords: Cardiomyopathies; Congenital abnormalities; Exercise; Isolated noncompaction of the ventricular myocardium
13/May/2019
Oral squamous papilloma: a view under clinical, fluorescence and histopathological aspects
DOI: 10.31744/einstein_journal/2019RC4624
ABSTRACT Oral squamous papilloma is a benign tumor whose pathogenesis has been associated with human papillomavirus infection. Thus, it is noteworthy that human papillomavirus infection is one of the risk factors associated with the development of cervical, anogenital, pharynx, larynx and oral cavity carcinomas. Oral squamous papilloma can affect any region of the oral cavity, and transmission of human papillomavirus can occur by direct contact, sexual intercourse or from mother to child during delivery. The diagnosis is clinical and histopathological, […]
Keywords: Fluorescence; Papilloma/diagnosis; Papilloma/pathology; Papillomaviridae; Pathology, oral
14/Feb/2019
Kaposi sarcoma of the penis in an HIV-negative patient
DOI: 10.31744/einstein_journal/2019RC4504
ABSTRACT Kaposi sarcoma is an angioproliferative disorder that ranges from a single indolent skin lesion to respiratory and gastrointestinal/visceral involvement. Kaposi sarcoma is rare in non-immunosuppressed patients. Nineteen cases of penile Kaposi sarcoma in HIV-negative patients were reported in 2012. We present the case report of a 48-year-old male patient with no previous medical history, who came to our urology clinic presenting a purple-color papule on the penis glans. Lab tests revealed negative serology for HIV, but tissue PCR was […]
Keywords: Herpesvirus 8, human; HIV; Penile neoplasms; Penis/pathology; Sarcoma, Kaposi
14/Feb/2019
Clinicopathological and immunohistochemical analysis of spindle cell squamous cell carcinoma of the tongue: a rare case
einstein (São Paulo). 14/Feb/2019;17(1):eRC4610.
View Article14/Feb/2019
Clinicopathological and immunohistochemical analysis of spindle cell squamous cell carcinoma of the tongue: a rare case
DOI: 10.31744/einstein_journal/2019RC4610
ABSTRACT Spindle cell squamous cell carcinoma of the tongue is a rare variant of squamous cell carcinoma. This paper reports the case of a spindle cell squamous cell carcinoma of the tongue, in a 64-year-old male patient, and presents a review of the etiopathogenesis, clinicopathological and immunohistochemical features and treatment of the malignancy. The patient presented for evaluation of a painful swelling on his tongue. Extraoral examination revealed palpable submandibular and superior cervical lymph nodes. Based on the presumptive diagnoses […]
Keywords: Carcinoma, squamous cell; Immunohistochemistry; Mouth/pathology; Tongue neoplasms/diagnosis
21/Nov/2018
Facial nerve hemangioma in the middle ear
DOI: 10.31744/einstein_journal/2018RC4509
ABSTRACT Facial nerve hemangioma is a rare and benign vascular tumor, and accounts for 0.7% of intratemporal tumors. We report the second case described in the literature of a facial nerve hemangioma in its tympanic segment. A 14-year-old male patient presented with a history of progressive right ear hearing loss with preserved facial mimicry. Pure tone audiometry showed a right ear moderate conductive hearing loss. Magnetic resonance imaging demonstrated an expansive lesion involving the tympanic segment of the right facial […]
Keywords: Ear, middle; Facial nerve; Hemangioma
21/Nov/2018
Severe iron-deficiency anemia as initial manifestation of pulmonary hemosiderosis in a child
DOI: 10.31744/einstein_journal/2018RC4505
ABSTRACT Idiopathic pulmonary hemosiderosis is a potentially fatal disease that results from episodes of alveolar hemorrhage of unknown origin. The clinical spectrum is varied, and anemia may constitute the only manifestation of illness, preceding other signs and symptoms by several months. We present the case of a 4 year-old child presenting with fever, vomiting and prostration, associated with pallor. He had microcytic and hypochromic anemia refractory to iron therapy. Gastrointestinal bleeding was ruled out after negative extensive etiological investigation. Subsequently, […]
Keywords: Anemia; Child; Hemosiderosis; Iron deficiency; Lung disease; Pulmonary diseases
30/Oct/2018
Late secondary urological reconstruction of separated ischiopagus twins with exstrophic bladder and urinary incontinence
DOI: 10.31744/einstein_journal/2018RC3887
ABSTRACT We report a case of secondary urinary reconstruction of previously separated conjoined twins with exstrophic bladder and urinary incontinence. Patients were male and aged 13-year-old. Twin one had a history of failed enterocystoplasty that extruded and was visible like an exstrophic neobladder. He underwent a procedure to close bladder neck and reconfigure abdominal wall. After the procedure the patient developed a fistula that was treated, but it persisted and, for this reason, a catheterizable pouch was constructed and native […]
Keywords: Reconstruction; Twins, conjoined; Urinary tract/surgery; Urologic surgical procedures