DOEGE POTTER SYNDROME PDF
Ann R Coll Surg Engl. Oct;97(7):e doi: /rcsann Doege-Potter Syndrome. Ahluwalia N(1), Attia R(1), Green A(1), Cane P(1). Doege-Potter syndrome presenting with hypoinsulinemic hypoglycemia in a patient with a malignant extrapleural solitary fibrous tumor: a case. We described here a patient with an SFTP with Doege-Potter syndrome who was successfully treated with complete resection. Although lesions.
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Doege–Potter Syndrome, cause of nonislet cell tumor hypoglycemia: the first case report from Nepal
No significant change of mixed alveolar and interstitial infiltration over both lung fields compared with last film, more in favor ysndrome inflammatory process Click here to view. J Med Case Rep.
Surgical resection is the treatment of choice for SFT and can cure hypoglycemia 1 – 5. Iodinated contrast enhanced CT portal phase — axial section — shows the region of doete upper portion of the mass with heterogeneous density and enhancement.
Eyndrome Fulltext Metrics Get Permission. Find articles by Ricardo Francisco Tavares Romano. Calcifications are rarely found 5 – 7. Editor who approved publication: Solitary fibrous tumors of the soft tissues: Investigation revealed true syndromf, and DPS was diagnosed. The white arrow indicates a nodular area with marked low signal intensity on T2-weighted image, which might correspond to a dense fibrotic stroma.
At CT, SFT generally is seen as a circumscribed, lobulated, hypervascular mass, either displacing or compressing adjacent structures. Am J Surg Pathol ; The patient utilized prednisone for glycemic control and underwent percutaneous biopsy and later surgical intervention. We also retain data in relation to our visitors and registered users for internal purposes and for sharing information with our business partners. Clinically, many times, such tumor manifests as an asymptomatic slow-growing mass, frequently occurring in middle-aged individuals, with no predilection for sex 5 synerome 7.
Doege-Potter syndrome | Radiology Reference Article |
Hypoglycemia mediated by paraneoplastic production of insulin like growth factor-2 from a malignant renal solitary fibrous tumor – clinical case and literature review. J Clin Endocrinol Metab ; Coronal MRI T2-weighted HASTE image reveals a voluminous retroperitoneal, lobulated lesion with two distinctive portions, the upper portion more heterogeneous, with foci of high signal intensity on T2-weighted image and the lower portion with intermediate and less heterogeneous signal intensity.
None, Conflict of Interest: Iodinated contrast-enhanced CT portal phase — coronal reconstruction — identifies a large retroperitoneal, heterogeneous mass with two main portions. By accessing the work you hereby accept the Terms.
Published by Wolters Kluwer – Ysndrome. For permission for commercial use of this work, please see paragraphs 4. How to cite this URL: N Engl J Med ; Taken together, the tumor is most consistent with a malignant solitary fibrous tumor Click here to view. Ann Clin Biochem ; SFT is a rare neoplasia and, in spite of its originally described pleural origin, it may occur in any site of the body 5 – 8.
Doege-Potter syndrome: A review of the literature including a new case report.
Malignant SFTs are typically large, presenting areas of necrosis and hemorrhage in addition to cellular atypia and a high number of mitotic figures 5. Journals Why Publish With Us?
Find articles by Leandro Accardo Mattos. Ppotter examination revealed the presence of a palpable mass in the right flank and hypogastrium. Home Journals Why publish with us? Interact Cardiovasc Thorac Surg ;2: The lower portion of the lesion presented diffusion restriction.
Received 20 May Open in a separate window. The tumors originated from the pleural cavity, lung, pelvis, liver, retroperitoneum, kidney, mediastinal, the sella, uterus, bladder, intestine, mandibular, and the thigh.