(This case study was added to OER Commons as one of a batch of over 700. It has relevant information which may include medical imagery, lab results, and history where relevant. A link to the final diagnosis can be found at the end of the case study for review. The first paragraph of the case study -- typically, but not always the clinical presentation -- is provided below.)

A 27 year old female patient, presented with left hemiparesis. Brain MRI showed multiple cystic ring-enhancing lesions involving the cerebrum and cerebellum (Figure-1A). She has received anti-tuberculous treatment for a recent diagnosis with pulmonary tuberculosis, however, the brain lesions showed with no response. Investigations revealed no other medical conditions. She underwent craniotomy and one of the lesions was excised from the left parietal lobe. It consisted of an oval white to gray soft tissue mass with solid white cut surface measuring 1.2x0.8x0.9cm (Figure-1B).

(This case study was added to OER Commons as one of a batch of over 700. It has relevant information which may include medical imagery, lab results, and history where relevant. A link to the final diagnosis can be found at the end of the case study for review. The first paragraph of the case study -- typically, but not always the clinical presentation -- is provided below.)

A 27-year-old woman was admitted to hospital with a 5-months history of difficulty in swallowing, hoarseness and increasing headaches since the last gestation trimester of her second pregnancy. Concerning her previous history, she reported that the same symptoms had occurred during the first gestation and had fully resolved after delivery. On neurological examination, a facial paresis and deafness were present on the right side. The patient also presented a significant dysfunction of the right IX, X and XI cranial nerves.

(This case study was added to OER Commons as one of a batch of over 700. It has relevant information which may include medical imagery, lab results, and history where relevant. A link to the final diagnosis can be found at the end of the case study for review. The first paragraph of the case study -- typically, but not always the clinical presentation -- is provided below.)

27-year-old lady with a history of upper extremity numbness and weakness.

(This case study was added to OER Commons as one of a batch of over 700. It has relevant information which may include medical imagery, lab results, and history where relevant. A link to the final diagnosis can be found at the end of the case study for review. The first paragraph of the case study -- typically, but not always the clinical presentation -- is provided below.)

The patient was a 27-year-old white male with a history of possible mild mental retardation attributed to traumatic brain injury at the age of 10. He was hospitalized at an outside hospital with several weeks of diffuse lower abdominal pain, mild dizziness and nausea, with approximately 50 pounds weight loss over an uncertain period of time. Four days after admission, he had deteriorating levels of consciousness, requiring intubation for airway protection. He was unresponsive to painful stimuli. Oculocephalic reflexes were absent. He had an upgoing Babinski response bilaterally. EEG showed diffuse generalized slowing. CSF showed 31 RBCs/cu mm, 2 WBCs/cu mm, 96 mg/dl glucose and 58 mg/dl protein. Despite multimodal therapy, the patient's neurologic condition did not improve. Due to a dismal prognosis for neurological recovery, a decision was reached with his family to switch to comfort measures only. The patient passed away 13 days after admission.

(This case study was added to OER Commons as one of a batch of over 700. It has relevant information which may include medical imagery, lab results, and history where relevant. A link to the final diagnosis can be found at the end of the case study for review. The first paragraph of the case study -- typically, but not always the clinical presentation -- is provided below.)

The patient is a 28 year old female who presented to an outside hospital with fatigue and easy bruising. She has a past medical history of cleft palate, type 2 diabetes, irritable bowel syndrome, and depression. She was found to have splenomegaly on physical exam. A complete blood cell count (CBC) was performed, which showed thrombocytopenia, borderline anemia, and neutropenia with a left shift. She was referred to a hematologist and a repeat CBC and bone marrow evaluation were performed:

(This case study was added to OER Commons as one of a batch of over 700. It has relevant information which may include medical imagery, lab results, and history where relevant. A link to the final diagnosis can be found at the end of the case study for review. The first paragraph of the case study -- typically, but not always the clinical presentation -- is provided below.)

28-year-old male with erythematous pruritic plaques with mild scales for a month, distributed over his left forearm, scrotum, left side waist and scalp (with alopecia).

(This case study was added to OER Commons as one of a batch of over 700. It has relevant information which may include medical imagery, lab results, and history where relevant. A link to the final diagnosis can be found at the end of the case study for review. The first paragraph of the case study -- typically, but not always the clinical presentation -- is provided below.)

In April 2006, a 28-year-old previously healthy man experienced headache, visual and aphasic speech disturbances. MR-imaging revealed a large, partly cystic mass of the left temporal lobe with significant contrast enhancement (Fig. 1). At surgical resection, due to infiltration of Wernicke's speech area, only subtotal tumor removal was achieved. Subsequent adjuvant therapy consisted of external beam radiotherapy (60 Gy) combined with temozolomide chemotherapy (75 mg/m2). After an uneventful clinical course of 14 months, a follow-up MRI in June 2007 showed a nodular and contrast-enhancing lesion at the anterior aspects of the former resection cavity. At subsequent craniotomy, the recurrent lesion could be dissected from cortical tissue circumferentially and gross total resection was achieved. Second-line chemotherapy with bevacizumab and irinotecan was initiated.

(This case study was added to OER Commons as one of a batch of over 700. It has relevant information which may include medical imagery, lab results, and history where relevant. A link to the final diagnosis can be found at the end of the case study for review. The first paragraph of the case study -- typically, but not always the clinical presentation -- is provided below.)

A 28-year-old woman presented with amenorrhea and blurred vision for 3 years and was admitted to our hospital for further evaluation. MRI of brain was performed and the coronal T2 weighted image revealed a well defined, high signal mass 26 x 22.5 x 21 mm, in the left anterior lobe of the pituitary gland. The pituitary stalk was elevated with of the hypothalamus (Figure 1). Serum prolactin level was 40.4 ng/ml (normal range: 3.0-20.0 ng/ml). The other results were within normal range. The preoperative survey revealed no evidence of other tumor in the body. The patient underwent transsphenoidal adenomectomy.

(This case study was added to OER Commons as one of a batch of over 700. It has relevant information which may include medical imagery, lab results, and history where relevant. A link to the final diagnosis can be found at the end of the case study for review. The first paragraph of the case study -- typically, but not always the clinical presentation -- is provided below.)

A 29 year-old male with limited health care interactions, previously diagnosed hypertension, and history of tobacco use presented following rapid onset nausea, dizziness, blurry vision, and tremors, resulting in a syncopal episode. At the initial formal assessment, physical examination revealed no specific abnormalities. Specifically, the neurologic examination demonstrated no focal deficits. Laboratory values were within normal limits, and toxicology studies were all negative. A CT scan of the brain revealed a 1.3 cm solitary, ring-enhancing lesion in the right temporal-parietal region, with associated vasogenic edema.

(This case study was added to OER Commons as one of a batch of over 700. It has relevant information which may include medical imagery, lab results, and history where relevant. A link to the final diagnosis can be found at the end of the case study for review. The first paragraph of the case study -- typically, but not always the clinical presentation -- is provided below.)

A 29-year-old man described progressive difficulty climbing stairs over a decade. He did not report any other neurological symptoms including upper limb, bulbar, facial or respiratory muscle weakness. His perinatal history and development were unremarkable, although he had never been particularly good at sport. There was no family history of cardiac or neuromuscular disease. Neurological examination revealed an exaggerated lumbar lordosis and myopathic gait. He had moderate symmetrical, predominantly proximal, limb weakness which was more marked in the lower than the upper limbs and normal tendon reflexes. There was no sensory loss, myotonia or muscle hypertrophy. Serum creatine kinase level was elevated at 1096 IU/L (upper limit of normal: 250 IU/L). Electromyogram was myopathic. Electrocardiogram and echocardiography were normal.

(This case study was added to OER Commons as one of a batch of over 700. It has relevant information which may include medical imagery, lab results, and history where relevant. A link to the final diagnosis can be found at the end of the case study for review. The first paragraph of the case study -- typically, but not always the clinical presentation -- is provided below.)

The patient is a previously healthy 29-year-old man who was admitted to our hospital for evaluation after experiencing seizures. A neurological examination elicited no abnormalities. CT and MR imaging were performed and revealed a cortico-subcortical lesion mass involving most of the right frontal lobe with sulcal effacement, compression on the foramen of Monro and hydrocephalus. The CT demonstrated curvilinear narrow calcifications (Figure 1). The lesion was hyperintense to the cortex on T2 and FLAIR (Figures 2 and 3) while partially hyperintense on T1 (Figure 4), with a marked homogeneous enhancement (Figure 5). All the sequences showed a "bag-of-worms sign" (which is best seen on the T2-weighted images) due to the presence of multiple tiny vessels associated with flow-voids (Figures 2 and 3). Moreover, in the lesion there were two deeply seated pseudocysts that showed contrast enhancement visible in the late phase. Based on these findings, a digital subtraction angiography (DSA) was performed which confirmed the hypervascular nature of the lesion but it did not indicate the presence of an arteriovenous malformation (Figure 6). At surgery, the lesion was removed via a right frontal craniotomy. The excision was macroscopically complete.

(This case study was added to OER Commons as one of a batch of over 700. It has relevant information which may include medical imagery, lab results, and history where relevant. A link to the final diagnosis can be found at the end of the case study for review. The first paragraph of the case study -- typically, but not always the clinical presentation -- is provided below.)

A 26-year-old man presented with a 1 year history of memory impairment. He became somnolence and lethargy 8 months before seeking medical attention. He needed to sleep over 20 hours per day. The physical examination and neurological examination were unremarkable.

(This case study was added to OER Commons as one of a batch of over 700. It has relevant information which may include medical imagery, lab results, and history where relevant. A link to the final diagnosis can be found at the end of the case study for review. The first paragraph of the case study -- typically, but not always the clinical presentation -- is provided below.)

The patient was a 29 year old Caucasian female with a past medical history of poorly controlled hypertension and diabetes mellitus who presented with a one week history of marked confusion and ataxia. She was brought to the hospital by local authorities who found her wandering in a nearby creek, completely disoriented with regards to where she was or how she had gotten there.

(This case study was added to OER Commons as one of a batch of over 700. It has relevant information which may include medical imagery, lab results, and history where relevant. A link to the final diagnosis can be found at the end of the case study for review. The first paragraph of the case study -- typically, but not always the clinical presentation -- is provided below.)

A 2-month-old male infant was referred to our hospital due to congenital hypotonia. The patient was normally delivered at 42 weeks of gestation age to a 20-year-old healthy mother. He was the first child of this family. Based on regular antenatal care, no abnormal findings were reported until birth when the APGAR scores at 1 and 5 minutes were 4 and 7, respectively. He had 2,850 g birthweight, 49 cm crown heel length, and 34 cm head circumference. The patient was hypotonic and had respiratory distress which required endotracheal intubation soon after delivery. Physical examination revealed generalized hypotonia. Myopathic facies without high-arched palate was noted. There was no evidence of metabolic disorders. Serum creatine kinase level was normal (56 IU/L). Serology tests for congenital infections were negative. SMN gene analysis displayed no mutation suggestive of spinal muscular atrophy. There was no evidence of consanguineous marriage in his family. The mother and her sister are clinically normal. The mother's male siblings passed away at 1 month and 1.5 months after birth due to respiratory distress complicated by respiratory infection (Figure 1).

(This case study was added to OER Commons as one of a batch of over 700. It has relevant information which may include medical imagery, lab results, and history where relevant. A link to the final diagnosis can be found at the end of the case study for review. The first paragraph of the case study -- typically, but not always the clinical presentation -- is provided below.)

A 2-year-old girl presented with one-month history of dysmetria and ataxia. Computer tomography (CT) of the brain showed a large parietal-occipital mass and marked hydrocephalus, for which she required placement of bilateral ventriculoperitoneal shunts. Magnetic resonance imaging (MRI) of the brain also revealed two nodules within the lateral ventricle (Figs. 1, 2 and 3, axial T1, non-enhanced T2, diffusion weighted imaging, respectively). Spine MRI showed abnormal leptomeningeal enhancement along the cervical spine, with additional enhancement in the thoracic and upper lumbar spine. A metastatic origin was excluded by exhaustive radiologic investigations, including body CT and positron emission tomography. Her disease progressed following completion of 6 months of intravenous and 3 months of oral chemotherapy; MRI showed interval increase in the size of the left temporal lobe ventricular lesions as well as worsening leptomeningeal disease and new parenchymal nodules. The tumor was completely excised and submitted for histopathological examination.

(This case study was added to OER Commons as one of a batch of over 700. It has relevant information which may include medical imagery, lab results, and history where relevant. A link to the final diagnosis can be found at the end of the case study for review. The first paragraph of the case study -- typically, but not always the clinical presentation -- is provided below.)

An O Rh(D)-positive term infant with intra-uterine growth restriction was delivered by elective C-section at 38 weeks to an O Rh(D)-positive G2P2 mother. The APGAR scores were 9 /10 at 1 minute and 9 /10 at 5 minutes. At birth, the baby was noted to have petechiae. Initial laboratory results confirmed severe thrombocytopenia (nadir 10,000/µL). The hematocrit, white cell (WBC) and red cell (RBC) counts were normal to low. Disseminated intravascular coagulation (DIC) was considered in the differential and antibiotics were initiated; however, the DIC workup showed normal fibrinogen levels, and cultures and viral testing for TORCH infections were negative.

(This case study was added to OER Commons as one of a batch of over 700. It has relevant information which may include medical imagery, lab results, and history where relevant. A link to the final diagnosis can be found at the end of the case study for review. The first paragraph of the case study -- typically, but not always the clinical presentation -- is provided below.)

A 2-year-old boy presented with gait imbalance and strabismus over the last two weeks. Five days before admission he began to vomit and became irritable. On admission a brain computed tomography was performed and revealed a large midline posterior fossa mass; the lesion was heterogeneous, cystic partly solid with calcifications (Figure 1). Magnetic resonance imaging that ensued demonstrated a 5x4.9x4.7cm mass within the 4th ventricle, extending through foramen of Luschka into the left cerebello-pontine angle without infiltration of the vermis (Figure 2). The lesion showed heterogenous enhancement after contrast administration (Figure 3). The patient was operated upon and a gross total resection of the mass was performed.

(This case study was added to OER Commons as one of a batch of over 700. It has relevant information which may include medical imagery, lab results, and history where relevant. A link to the final diagnosis can be found at the end of the case study for review. The first paragraph of the case study -- typically, but not always the clinical presentation -- is provided below.)

A previously healthy 2-year-old boy presented with one to two days of anuria and bloody diarrhea. He was admitted to the local children's hospital with a diagnosis of hemolytic uremic syndrome (HUS), presumably secondary to E. coli O157 but never confirmed. Laboratory studies revealed hemolysis, renal failure and thrombocytopenia. Eleven hours after admission, his blood oxygen saturations worsened and he was intubated. He was then noted to have fixed and dilated pupils. A head CT was performed, which revealed left frontal subcortical white matter vasogenic edema with left frontal gyral hyperdensity, as well as scattered pockets of pneumocephalus (Figure 1). Pneumocephalus without evidence of a calvarial fracture raised concern for an infectious process. Left-to-right midline shift with effacement of the cisterns and left uncal herniation were also observed. Neurosurgical consultation advised that no intervention was possible. The patient became bradycardic and required resuscitation, which unfortunately was not successful. He expired 14 hours after being admitted to the hospital. Ante-mortem bacterial blood cultures were positive.

(This case study was added to OER Commons as one of a batch of over 700. It has relevant information which may include medical imagery, lab results, and history where relevant. A link to the final diagnosis can be found at the end of the case study for review. The first paragraph of the case study -- typically, but not always the clinical presentation -- is provided below.)

This 2-year-old male was referred to a Genetic Counselor at the age of 22 months for developmental delay and dysmorphic features.

(This case study was added to OER Commons as one of a batch of over 700. It has relevant information which may include medical imagery, lab results, and history where relevant. A link to the final diagnosis can be found at the end of the case study for review. The first paragraph of the case study -- typically, but not always the clinical presentation -- is provided below.)

A 2-year old girl presents with a liver mass. The mass is unifocal and multi-lobulated on imaging and occupies the entire right lobe, displacing the main branches of the portal veins. The serum alpha-fetoprotein is elevated to 680 ng/dL and the only other pertinent finding is an elevated platelet count to 685,000. An open biopsy is performed and representative sections are displayed below: