CLINICAL HISTORY 10

CLINICAL HISTORY 1

A 5 month-old male infant John McConnwale was brought to the Emergency Department by his parents with persistent, worsening shortness of breath and wheezing associated with excitement and physical exertion. The boy was lethargic, anorexic. He had a history of poor sleep and crying for two days. No fever, diarrhea, vomiting, foreign-body ingestion were noted. No asthma, recent illness or antibiotic ingestion, home treatment, recent infectious exposure or immunizations were recorded. There was evidence of dehydration, with limited tearing and decreased urine output. Oral intake was limited.

A chest Computed Tomography showed large, thin-walled cysts occupying most of the left hemithorax. A small portion of collapsed lung was present in the left upper thorax. The largest cyst was approximately 8 cm. There was a significant mass with mediastinal shift to the right. The right lung was essentially clear. There was no evidence of pneumothorax. The impression was of congenital cystic malformation of the lung.

CLINICAL HISTORY 2

A 21-year old Caroline Montley, student of Law University had 5 episodes of wheezing attacks during her childhood associated with mumps, chicken-pox, and common colds. After a move to the California coast at the age of 13, she had no asthmatic symptoms up to the present case. She is in distress, with labored breathing. The patient has a sensation of chest constriction. She produces coarse dry rales in the bronchial tubes. She thinks that continual wheezing and mild dyspnea are connected with relatively cold and damp months, at times with the periods of emotional upset, and after exposure to tobacco smoke. The symptoms are not aggravated by exposure to animal or house dust. The physical examination reveals increased resonance to percussion. Chest X-ray films show marked abnormalities.

CLINICAL HISTORY 3

A 2-year-old boy Jacob Witch was brought to the local General Practitioner by his mother. After the medical examination he was immediately referred to the city hospital. Five days before the admission he began to vomit and became irritable. He had a bad weakness, sweating and malaise.

On the admission a brain Computed Tomography was performed which revealed a large midline mass; the lesion was heterogeneous, cystic, partly solid with calcifications. Magnetic resonance imaging demonstrated a 5x4.9x4.7cm mass, extending into the left angle. The patient was operated upon and a total resection of the mass was performed.

CLINICAL HISTORY 4

A 34-year old school teacher of Geography Julia Mettew came to one of the clinics complaining of bad headaches and generalized malaise which lasted out. The temperature was 38,4º, the pulse rate 120, and the respiration 27 per minute. The throat was acutely inflamed and edematous and both tonsils were covered with an exudate. The patient was hospitalized and on the tenth day when the throat appeared normal and her ward doctor thought that the temperature should decrease too, it continued to be elevated and the woman complained that she could not swallow at all. A few hours later she refused to take the food. Local examination at this time revealed a swelling on the anterior surface of the neck above and in the region of the thyroid gland. The patient’s complaint that she could not swallow was confirmed by having her drink water under the observation: each time that she attempted to swallow it, the water came through her nose. A diagnosis of abscess of the prevertebral fascial space was made and the operation was performed. An incision, three and a half inches in length, was made. An aspirating needle was inserted into the mass and thick creamy pus was evacuated. The recovery was uneventful and the patient was discharged ten days later.

CLINICAL HISTORY 5

A 16 month old female Cristina Horthex was admitted to the Pediatric Intensive Care Unit with fever, hypoxia, altered mental status, breathlessness, and seizures. Magnetic resonance imaging (MRI) of the brain showed a single intraventricular mass which could be isolated easily because of dense cells concentration. The mass measured 4x4x4 cm. There was additional, but mild right lateral ventricular dilatation. These characteristics were most suggestive of a meningioma.

The patient subsequently had surgical resection of the mass with MRI Navigation Guidance. The mass had a thick capsule and a rubber like core. The tumor was removed without intraoperative complications. The patient was discharged home 4 days later and had done well since that time with no neurological disorders.

The child's parents underwent extensive genetic counseling and were encouraged to undergo mutation analysis as both are in their early twenties.

CLINICAL HISTORY 6

A pregnant woman Monica Lux, aged 19, had two spontaneous early abortions. On clinical grounds delivery was expected in the middle of February. The present pregnancy ran a normal course. On December 8, when the pregnancy was estimated to have lasted approximately 32 weeks, the patient was hospitalized for probable fetus growth retardation and mild vaginal blood loss. In spite of treatment and a salt-free diet the blood pressure rose up to 170 over 110 and the patient had constant sense of nausea. On December 12, 06.15.am, the patient had a few contractions, the base line of the fetal heart rate was 155 to 160 beats per minute. On December 13, 11.35.am, the fetal heart sounds could no longer be heard and a female dead fetus, weighing 1600 grams, 31 cm longer was delivered. There were no congenital abnormalities. The placental weight was 230 grams. There was noticed an important ischemic necrosis with vascular necrosis.

CLINICAL HISTORY 7

The patient is a 6-year old girl, Bernarda Crix, with past medical history significant for biliary cirrhosis. The patient, at one year of age, underwent a liver transplantation. This time she is admitted with an enlarging left neck nodal mass.

On admission significant laboratory findings include:

Hemoglobin-12.2g/dL;

Increased white blood cell count with:

Neutrophiles-49%,

Lymphocytes-31%,

Monocytes-9%,

Eosinophils-10%,

Basophils-1%.;

Renal function tests, electrolytes, glucose-within normal limits.

The examination reveals two partially affected practically equal in size lymph nodes matted together (4.5 x 2.5 x 1.5 cm).

CLINICAL HISTORY 8

A 45-year-old electrician Kent Renou fell 3 meters on January 5 and was unconscious for 15 minutes. He was found by his neighbours and wife and admitted to the hospital where after regaining consciousness, he complained of pain in both shoulders and neck and of numbness of the second and third fingers of the right hand. He was noted to have limitation of neck motion. A cervical spine roentgenogram, taken at the time of his admission, included only five upper vertebrae. A complete roentgenographic series of the cervical spine taken the next day was normal. He was treated by physiotherapy and discharged several days later.

His complaints persisted and two months later a consultation revealed a tilt of his head to the right, limitation and diffuse tenderness of the posterior neck muscles. The right triceps reflex was absent with hypoesthesia to pin prick over the second and third fingers of the right hand. A lateral cervical X-ray film demonstrated a first-degree delayed traumatic dislocation of the cervical spine. An anterior cervical disk-ectomy and reduction of the cervical vertebrae were performed. The patient did well and was asymptomatic ten months later with roentgenographic evidence.

CLINICAL HISTORY 9

A 3-year-old girl Marisha Pishka with a history of mild motor delay was presented with a change in mental status, gait difficulties, nausea and vomiting. The patient was in her usual state of health until 9 months prior to presentation, when she was found to have abnormalities of the left eye. Over the next several months, she developed gait difficulties and behavioral changes. On the day of admission, she developed confusion, severe gait difficulties, nausea and profuse vomiting. On physical examination, she had increased deep tendon reflexes of her right Achilles tendon. She subsequently became unresponsive. She was intubated and given mannitol and steroids. An external ventricular drain was placed. Neuroimaging showed a minimally heterogeneous tumor measuring 8×8×9 cm involving the left parietal region and, partly filling the left lateral ventricle. Gross total resection of the tumor was confirmed by post-operative imaging. Staging evaluation revealed no metastasis. The patient was discharged one week later.

CLINICAL HISTORY 10

The patient Robert Bush was born at 38 weeks via C-section. The pregnancy was complicated by gestational diabetes in the mother who was treated. She also had elevated liver function tests (LFTs) during pregnancy; otherwise, no additional problems were noted. He was 7 pounds 14 ounces. The patient was diagnosed with neonatal jaundice, treated with phototherapy and discharged three days after birth.

This baby boy with postnatal onset microcephaly had speech impairment and global developmental delay that were noted at 12 months of age. He also had feeding problems which included gagging, choking and frequent drooling. The mother also noted that the child has been sleeping more in recent weeks. According to the mother, the infrequent episodes are typified by the boy stopping suddenly, staring and becoming unresponsive. The child's history is negative for convulsions, meningitis, encephalitis or severe head trauma associated with loss of consciousness. There is no family history of developmental delay or neurological problems. The boy is characterized by frequent smiling and laughter, hyperactivity. He has a strikingly pale hair and unusually pale blue eyes. Involuntary hand movements, wide-based gait, and dystonically upgoing toes are noticed. The patient's physical examination is positive. An EEG was performed and showed a normal awake-and-asleep pattern; however, a subtle slow background frequency for age was noted. An MRI was positive. A blood sample from the patient was sent for DNA molecular testing.

Date: 2015-12-11; view: 1330