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Unusual Site (unusual + site)

Distribution by Scientific Domains
Medical Sciences88%

Selected Abstracts

Left Atrial Appendage Tip: An Unusual Site of Successful Ablation After Failed Endocardial and Epicardial Mapping and Ablation

JOURNAL OF CARDIOVASCULAR ELECTROPHYSIOLOGY, Issue 2 2010
LUIGI DI BIASE M.D.
Left Atrial Appendage Tip. Uncommon sites of ablation for arrhythmias can be the cause of failed ablations. This series includes 4 cases requiring ablation at the tip of the left atrial appendage after both endocardial and epicardial mapping and ablation failed. (J Cardiovasc Electrophysiol, Vol. 21, pp. 203-206, February 2010) [source]

Tumoral Calcinosis of the Scalp: An Unusual Site for a Rare Tumor

THE LARYNGOSCOPE, Issue 1 2007
Jubbin Jagan Jacob MD
Abstract Tumoral calcinosis is a rare calcifying disorder that is associated with deposition of calcium crystals in the periarticular tissues. The mass is most often around the hips, elbows, shoulders, and feet but may be occasionally found elsewhere. We report a case of multiple sporadic tumoral calcinoses in an adult male over the scalp. The scalp as a site of tumoral calcinosis has not been previously reported in adults. Previous surgical excisions done on two occasions had resulted in recurrence of the tumors. This report highlights the need to include tumoral calcinosis in the differential diagnosis of tumors of the scalp. [source]

Cytodiagnosis of benign fibrous histiocytoma of rib and diagnostic dilemma: A case report

DIAGNOSTIC CYTOPATHOLOGY, Issue 6 2010
Santosh Kumar Mondal M.D.
Abstract Benign fibrous histiocytoma (BFH) of bone is rare in occurrence, and rib is an unusual site. There are limited case reports of this entity in the literature, and cytodiagnosis of this tumor is not described. A 24-year-old man presented with a firm mass and pain in the right lateral chest wall. Radiological investigations (plain radiograph and computed tomography) revealed a lytic bone lesion involving the 5th rib. Radiologically, giant cell tumor (GCT), BFH, and plasmacytoma were suspected. In fine-needle aspiration cytology (FNAC), admixture of benign stromal cells and scattered osteoclast type giant cells were found in the smears. Differential diagnoses of BFH, GCT (non-epiphyseal type), fibrous dysplasia, and aneurysmal bone cyst were made on cytology. Subsequent histologic examination confirmed the diagnosis of BFH. Cytologic diagnosis of BFH of rib is difficult as this tumor may mimic other giant cell containing tumors of bone in FNAC. The final diagnosis should always be made after correlation with histological, radiological, and clinical features. Diagn. Cytopathol. 2010. © 2009 Wiley-Liss, Inc. [source]

Malignant pheochromocytoma with progressive paraparesis in von Hippel,Lindau disease

EUROPEAN JOURNAL OF NEUROLOGY, Issue 4 2000
R. Mössner
Pheochromocytomas are a feature of the von Hippel,Lindau disease spectrum, a multisystem disorder of autosomal dominant inheritance. Pheochromocytomas are, however, observed during life with a lower frequency than other features of this disease, such as retinal angiomas, haemangioblastomas of the CNS, and renal carcinomas. We present the highly unusual case of a patient who required an emergency operation for an intradural extramedullary thoracic tumour which was clinically suggestive initially of neurinoma. We present evidence from NMR, histological and isotope scan investigations of this being a pheochromocytoma metastasis and of an additional right-sided paraganglioma at the same height. A detailed history revealed that this patient had suffered from four other pheochromocytomas and two other paragangliomas, in addition to retinal angiomatosis of von Hippel,Lindau disease. This case is extraordinary due to (i) the unusual site of the metastasis, (ii) the neurological requirement for an emergency operation of pheochromocytoma, (iii) metastasis of pheochromocytoma in von Hippel,Lindau disease (only eight previous cases), and (iv) the number of recurrent pheochromocytomas. It clearly demonstrates the necessity for frequent and life-long follow-up in von Hippel,Lindau disease. [source]

Number, Spoils, and Relics: Totemic Images in aMnemotopia

JOURNAL OF ARCHITECTURAL EDUCATION, Issue 1 2000
Ann Marie Borys
At northern Italian Counter-Reformation pilgrimage sites known as sacri monti (sacred mountains), the traditional focus on a site made sacred by events of religious importance is replaced by a condition of exile to a remote and difficult landscape. Judith Wolin argues thatsacri monti as a group can be understood as mnemotopias, "memory places," whose primary function "is to allow the revisitation of ,remembered' events." An unusual site with similar intentions, designed in the 1590s by Vincenzo Scamozzi as part of a villa project, shares some defining qualities ofsacri monti. Yet Scamozzi's project is unique; the goal of this paper is to show how Scamozzi participates in the mnemotopic tradition without employing explicit representational narrative. In its place stand number correspondence, a narrative use of the orders, and a layered speculation on bodies and fragments. [source]

Diffuse-type giant cell tumor/pigmented villonodular synovitis arising in the sacrum: Malignant form

PATHOLOGY INTERNATIONAL, Issue 9 2007
Yoshinao Oda
Diffuse-type giant cell tumor (GCT)/pigmented villonodular synovitis (PVNS) in the axial skeleton or spine is rare. Herein is reported a case of diffuse-type GCT/PVNS involving the sacrum and the fifth lumbar vertebra, in which the patient developed regional lymph node swelling after recurrence. The recurrent tumor was found to have atypical histological features such as spindle cell morphology, cytological atypia and high mitotic rate, which are compatible with the diagnostic criteria of secondary malignant diffuse-type GCT/PVNS. Although the nodal lesions were not sampled histologically, the clinical and histological features indicate that the current case is an example of malignant diffuse-type GCT/PVNS. This case is considered to be the first case of malignant diffuse-type GCT/PVNS in the spine, because no such lesions have been previously reported in the axial skeleton or spine. Careful surveillance should be required for diffuse-type GCT/PVNS arising at unusual site. [source]

Life Threatening Hemorrhage From Osteoradionecrosis of the Ribs and Clavicle

THE LARYNGOSCOPE, Issue 9 2007
MRCS, Mohammed Iqbal Syed MD
Osteoradionecrosis (ORN) is a familiar complication of radiotherapy. ORN of the clavicle and ribs is well documented after radiation therapy for breast and pulmonary malignancy. ORN of the clavicle after radiation therapy to the neck is very rare. We report the first case in which both clavicles and first ribs underwent ORN 14 years after neck irradiation and surgery for laryngeal malignancy. The presentation was atypical; erosion of the right internal mammary artery causing life-threatening hemorrhage. Otolaryngologists should be aware that ORN can occur at an unusual site and can have an atypical presentation. [source]

Relevance of translocation type in myxoid liposarcoma and identification of a novel EWSR1-DDIT3 fusion

GENES, CHROMOSOMES AND CANCER, Issue 11 2007
B. Bode-Lesniewska
The clinical course of myxoid/round cell liposarcoma (MRCL) is characterized by frequent local recurrences and metastases at unusual sites. MRCLs carry specific translocations, t(12;16) or rarely t(12;22), linking the FUS or the EWSR1 gene with the DDIT3 gene, respectively. Nine FUS/DDIT3 and three EWSR1/DDIT3 variants of fusion transcripts have been described thus far. In search of prognostic markers for MRCL, we analyzed the translocation types of 31 patients and related them to the event free and overall survival. Using break-apart FISH and RT-PCR combined with DNA sequencing, we detected FUS/DDIT3 fusions in 30 sarcomas, while an EWSR1/DDIT3 translocation was identified in one tumor. FUS/DDIT3 type II (exons 5-2) was most commonly detected (20 cases), followed by type I (7-2) (7 cases) and type III (8-2) (3 cases). A single tumor carrying a t(12;22) translocation expressed a hitherto unknown EWSR1-DDIT3 fusion transcript (13-3) linking the complete RNA-binding domain of EWSR1 with a short piece of the 5,-UTR and the entire open reading frame of the DDIT3 gene. Interestingly, five of six patients with type I (7-2) FUS/DDIT3 fusions displayed local recurrences and/or metastatic spread within the first 3 years, generally requiring chemotherapeutical treatment (median disease-free survival 17 months). In contrast, 9 of 13 patients with type II FUS/DDIT3 translocations remained at 3 years disease-free (median disease-free survival 75 months). Since the total number of patients is still limited, further studies are required to verify a putative association of type I FUS/DDIT3 -fusion transcripts with a prognosis of MRCL. © 2007 Wiley-Liss, Inc. [source]

Intramuscular spindle cell lipoma: Case report and review of the literature

PATHOLOGY INTERNATIONAL, Issue 4 2001
Keisuke Horiuchi
Spindle cell lipoma (SCL) is a relatively rare adipocytic neoplasm and is histologically characterized by a mixture of uniform spindle cells and mature fat cells. It occurs predominantly in male patients aged 45,65 years, and in most cases it arises in the subcutaneous tissue of the neck or shoulder. Although the neoplasm sometimes affects unusual sites, only three cases have been reported in which the lesion was intramuscular. Here we present a case of SCL arising in skeletal muscle; to our knowledge, the first report in 10 years. The tumor occurred in the neck of a 50-year-old male patient. Magnetic resonance imaging (MRI) revealed a lipomatous tumor within the right trapezius muscle. The tumor was localized beneath the fascia and was excised completely at surgery. Histologically, the tumor was typical of a spindle cell lipoma with no evidence of malignancy. An immunohistochemical study revealed all spindle cells were strongly positive for CD34. Differential diagnosis is discussed with a review of the literature. [source]