Pregnancy- and lactation-associated vertebral compression fractures: MRI prevalence and characteristics.

The frequency of pregnancy- and lactation-associated vertebral compression fractures (PLVCFs) is not known. This study showed that MRI prevalence of PLVCFs was approximately 0.5% in females ≥ 15 and < 40 years of age over a 48-month period. PLVCFs did not display MRI features distinguishing them from other vertebral insufficiency fractures. PURPOSE: We aimed to investigate the MRI prevalence and characteristics of pregnancy- and lactation-associated vertebral compression fractures (PLVCFs). METHODS: This retrospective cross-sectional observational study included all thoracic, lumbar, or thoracolumbar MRI examinations performed in our hospital (or at outside centers and referred to us for consultation) of females ≥ 15 and < 40 years of age during a 48-month period. Two radiologists independently reviewed all images for vertebral compression fractures and their disagreement was resolved by a third blinded senior radiologist with 24 years of dedicated musculoskeletal radiology experience. MRI features of PLVCFs (early/late stage, height loss, endplate involvement, retropulsion) were noted. RESULTS: A total of 1484 MRI examinations-including 50 consultations from outside centers-of 1260 females (mean age, 27.7 years; range, 15-39) were included. Interobserver agreement of the two junior radiologists was substantial (κ = 0.607; 95% CI, 0.545-0.669). Vertebral compression fractures were identified in 177 of thoracic (n = 210), lumbar (n = 900), or thoracolumbar MRI (n = 374) examinations. Six women (7 MRI examinations; 4.0% of MRIs with vertebral fractures) had PLVCFs diagnosed on MRI (prevalence, 0.47%; mean age, 31 years; age range, 25-37). Number of fractured vertebrae in cases with PLVCF ranged between 1 and 11 (mean, 5.6). DEXA, available in all patients with PLVCFs, verified osteopenia/osteoporosis in four of six patients. CONCLUSION: PLVCFs have an MRI prevalence of approximately 0.5% in the target population and do not display distinguishing features from other insufficiency type vertebral compression fractures.

MRI of a benign chondroid syringoma.

Chondroid syringoma, also known as mixed tumour of the skin, is a relatively rare, usually benign tumour. A few malignant cases, especially in the lower extremities, have been published, but most of them behave in a benign fashion. A case of a middle-aged woman with surgically proved chondroid syringoma in the pretibial region is presented in this report with MRI and histological findings. Despite rapid growth over a short period of time and a location reportedly associated with malignancy, the histological features were benign.

Change in the amputation profile in diabetic foot in a tertiary reference center: efficacy of team working.

Diabetic foot is a serious complication of diabetes mellitus and the risk of lower extremity amputation is very high in this population when compared with people without diabetes. We have previously reported the lower-extremity amputation rate and significant factors in determining the risks for patients who had been admitted to Hacettepe University Hospital, a tertiary reference center for Turkey, between the years 1992 and 1996. In January 2000, a diabetic foot care team including an infectious diseases specialist, orthopaedic surgeons, endocrinologists, a plastic and reconstructive surgeon, a radiologist, and a diabetic foot nurse was assembled. To determine whether a change has occurred in the rate and the risk factors of lower extremity amputations after the establishment of this team, medical records of 66 patients (39 men, 27 women) with diabetic foot who had been admitted to Hacettepe University Hospital between 2000 and 2002 have now been retrospectively analysed. The grade distribution of diabetic foot according to Wagner classification was quite similar in the two studies (grade 1: 0 % vs. 4.5 %, grade 2: 15.6 % vs. 19.7 %, grade 3: 48 % vs. 33.3 %, grade 4: 24.4 % vs. 30.3 %, grade 5: 11.5 % vs. 12.1 % in the former and current study, respectively). The overall amputation rate in the current study was 39.4 % (36.7 % in the former study). Ray amputation (35 %) and below-knee amputations (30 %) were the two most commonly applied procedures. The rates of Syme, above knee, other amputations (i.e., Boyd, talonavicular amputations and partial calcanectomy) were 8 %, 8 % and 19 %, respectively. These data suggest that amputation is still a frequently encountered outcome for our patients with diabetic foot, but the amputation profile has changed. The implementation of a diabetic foot care team has relatively decreased the rate of major amputations in an attempt for limb salvage to improve the quality of life of the patients. Presence of osteomyelitis, peripheral vascular disease and gangrene still remain as significant predictors of amputation in our population.

Water-lily sign on MR imaging of primary intramuscular hydatidosis of sartorius muscle.

Primary hydatidosis of muscle is very rare and can cause a variety of diagnostic problems, especially in the absence of typical radiologic findings. This is the report of a case of primary intramuscular hydatid cyst in a 35-year-old woman, who presented with a 1-year history of a painless lump in the distal left thigh. The authors document the pathognomonic water-lily sign that has not previously been reported in a case of intramuscular hydatid disease.

Bilateral discoid medial menisci: association with bone changes in the tibia.

We present here the third case report of bilateral discoid medial menisci with associated bone changes. An 18-year-old man had bilateral medial tibial plateau depression (cupping) accompanying medial discoid menisci documented by magnetic resonance imaging and confirmed by arthroscopy. The patient was treated successfully by excision of the torn central anomalous discoid portion of the menisci using arthroscopic partial resection technique.

MR imaging of the acetabular labrum: a comparative study of both hips in 180 asymptomatic volunteers.

The aim of this study was to determine the MR imaging characteristics of normal acetabular labra on both hips. Three hundred sixty acetabular labra on both hips of 180 asymptomatic volunteers were examined on a 0.5-T MR unit utilizing a superficial coil. T1-weighted and T2-weighted gradient-echo sequences (TR/TE/FA 169/10 ms/40 degrees, and 316/25 ms/40 degrees, respectively) were used. The volunteers were classified into five age groups (10-19, 20-29, 30-39, 40-49, and 50 + years of age). The shape (triangular, flat, round, absent), size, and the presence of intralabral foci of increased intensity (diffuse, linear, central, or basal) were noted on both labra in each volunteer, and symmetry-asymmetry of these features were investigated. The most common labrum shape was triangular, whereas absence of labrum was the least common condition. A difference of labral shapes between both hips was present in approximately 15% of volunteers. A size difference of over 25% between each labrum was noted in approximately one-fourth of volunteers. An age-related pattern of intralabral intensity increase was noted on both MR sequences (more commonly on T1-weighted gradient-echo images). Shape differences and age-related intensity changes of the acetabular labrum in the MR imaging of the hips were confirmed, and the possibility of variability of the labra, with regard to the shape and size, on both hips of the same individual was documented.

MR imaging of pelvic and thigh muscles in congenital muscular dystrophy.

To define and compare the magnetic resonance (MR) imaging findings of pelvic and thigh muscles in merosin-deficient and merosin-positive congenital muscular dystrophy, 10 patients with merosin-positive and six patients with merosin-deficient muscular dystrophy were examined in a 0.5 T MR imaging unit. Intensity and atrophy scores were given to individual muscles by two radiologists and were calculated for three muscle groups (pelvic, anterior thigh and posterior thigh muscles). Rectus femoris was affected less than the vastus muscles in 40 percent of cases in merosin-positive patients, whereas there was no selective sparing in merosin-deficient patients. Sartorius and gracilis were relatively spared in both groups. The most consistently affected muscles were gluteus maximus, adductor magnus and brevis in merosin-positive patients. Atrophy was more prominent in the adductor muscles in the merosin-deficient group. Intensity scores of anterior thigh muscles of the merosin-positive group were significantly higher than those of the merosin-deficient group (U = 8, p = 0.016). When stepwise logistic regression model was applied, intensity score of the anterior thigh muscles was found to be the best differentiating variable. The regression analysis model formed was able to differentiate the two forms with a sensitivity of 80 percent and specificity of 83 percent.

Normative measurements of orbital structures using MRI.

PURPOSE: The purpose of this work was to establish criteria for the diameters of normal extraocular muscles and superior ophthalmic vein and width of the optic nerve-sheath complex, to determine normal globe position as seen on MRI, and to investigate the effects of age and sex on these structures. METHOD: Diameters of the extraocular muscles and superior ophthalmic vein, width of the optic nerve-sheath complex, and distance from the interzygomatic line to the posterior margin of the globe were calculated for 200 normal orbits of 100 patients on T1-weighted MR scans. RESULTS: Normal ranges for diameters of the extraocular muscles were as follows (mean +/- 2 SD): medial rectus, 3.2-4.9 mm; lateral rectus, 2.6-4.8 mm; inferior rectus, 3.7-6.0 mm; superior group, 3.1-5.6 mm; superior oblique, 2.4-4.1 mm. The normal position of the posterior pole of the globe was 8.9 mm behind the interzygomatic line (range 5.0-12.7 mm). The mean diameters of the extraocular muscles in male patients were significantly larger than those in female patients (p < 0.001). CONCLUSION: These data may be of value in quantitatively evaluating MRI of the orbit.

Cerebellar and basal ganglion involvement in Langerhans cell histiocytosis.

Langerhans cell histiocytosis (LCH) is a disease of unknown cause characterised by proliferation of histiocytic granulomas in tissues; the primary cerebral manifestation is diabetes insipidus caused by hypothalamic infiltration. We present a patient in whom, except for the absence of high signal on T1 weighting in the posterior pituitary, consistent with central diabetes insipidus, MRI showed no evidence of hypothalamic involvement by histiocytosis, despite the long duration of the disease. However, there was bilateral, symmetrical involvement of the cerebellum and globus pallidus in addition to a calvarial lesion. High signal in the cerebellar white matter on T2-weighted images may represent demyelination, gliosis and cell loss, as previously reported on pathologic examination.

Central nervous system involvement in incontinentia pigmenti: cranial MRI of two siblings.

Incontinentia pigmenti is an uncommon neurocutaneous syndrome characterised by skin lesions, dental and ocular abnormalities and central nervous system involvement. We report the cranial MRI findings in two sisters with this condition. These include hypoplasia of the corpus callosum, enlargement of the lateral ventricles and periventricular white-matter lesions. One girl also had unilateral microphthalmia and rostral agenesis of the corpus callosum, a feature not previously described.

CT and MRI of microcephalia vera.

CT and MRI findings in three patients, two of them siblings, with microcephalia vera are presented. In this rare entity, a very small brain with an extremely thin, smooth cortex and increase surrounding cerebrospinal fluid are observed.

Pseudotumor formation in tibia in Gaucher's disease.

A very rare case of type 1 Gaucher's disease with pseudotumor formation in the right tibia is presented. In addition to the characteristic radiographic finding of distal femoral flaring (Erlenmeyer flask deformity), a lobulated osteolytic area with surrounding sclerosis was seen in the proximal metaphysis of the right tibia. Adjacent to this pseudotumor appearance was an old pathologic fracture and no significant soft tissue swelling was evident, both of these features being reported for the first time in association with Gaucher's disease.

MR imaging in squamous cell carcinoma of the head and neck with no palpable lymph nodes.

PURPOSE: To assess the efficacy of MR imaging in the detection of lymph node metastasis in patients with no palpable lymph nodes ("N0 neck") who have squamous cell carcinoma of the head and neck region. MATERIAL AND METHODS: MR neck imagings in 18 patients who underwent neck dissection (bilaterally in 2) for squamous cell carcinoma of the head and neck region were examined preoperatively for the purpose of detecting lymph node metastases. The imaging features taken into consideration were: size (cutoff point 10 mm), grouping, presence of central necrosis, and appearance of extracapsular spread. The MR examinations comprised spin-echo T1- and T2-weighted sequences. The MR findings were compared with those of surgery and histopathological examination. RESULTS: MR suggested metastatic lymph node involvement in 5 necks. In 2 of these, central necrosis was seen in the enlarged lymph nodes. In a third, a grouping of the lymph nodes was noted. Extracapsular spread was not present. Histopathological examination revealed metastatic lymph nodes in 7 of the 20 necks, the rate of clinically occult disease being 35%, and 4 of them had been accurately graded by MR. There was one false-positive MR examination. The MR sensitivity was 57.1% and specificity 92.3%. CONCLUSION: MR may reveal metastatic lymph nodes in patients with no clinical evidence of metastasis. However, conventional MR techniques are not always sufficient for decision-making on surgery in cases of "N0 neck".

Calcium within a bronchogenic cyst with a fluid level.

A 38-year-old man presented with a bronchogenic cyst which showed a high calcium content. The calcium precipitate layered in the dependent part of the cyst to form a fluid level. The CT and MRI findings of this rare case are discussed.

Rhombencephalosynapsis associated with hand anomalies.

A case of rhombencephalosynapsis, a very rare disorder characterized by agenesis or hypogenesis of the cerebellar vermis and fusion of the cerebellar hemispheres, is reported with magnetic resonance imaging features. Radiographs showed anomalies in both hands; namely phalangeal hypoplasia and occult polydactyly in the right hand and syndactyly in the left, previously unreported in association with this disorder.

Urethro-vaso-cutaneous fistula in a 5-year-old child.

A 5-year-old boy with a 4-year history of urethro-vaso-cutaneous fistula is presented. This is the youngest patient reported to have an acquired urethro-vaso-cutaneous fistula. Fistulography is a convenient method for the demonstration of such entities.