排序方式: 共有15条查询结果,搜索用时 15 毫秒
1.
2.
3.
4.
Vimal Kumar MD FNB Dhanalakshmi Angappan MD Deenadayalan Munirathnam DCH DNB FNB Mukul Vij MD PDCC 《Pediatric dermatology》2017,34(6):732-734
Langerhans cell histiocytosis (LCH) is a multisystem disorder involving various organs. Nail changes in LCH are extremely rare. We present this case report of extensive nail changes in an 18‐month‐old child with multisystem LCH. 相似文献
5.
6.
7.
Two cases of primary non‐Hodgkin's lymphoma of female breast: Role of fine‐needle aspiration cytology and cell‐block immunohistochemistry
下载免费PDF全文
![点击此处可从《Diagnostic cytopathology》网站下载免费的PDF全文](/ch/ext_images/free.gif)
Tarak Banik M.D. DNB PDCC CYTOPATH. Krishnendu Mondal M.D. Rupali Mandal M.D. 《Diagnostic cytopathology》2016,44(3):235-240
Primary breast lymphoma (PBL) is an uncommon neoplastic condition. Though HIV‐infection is a known risk factor for the development of extranodal lymphomas, mammary involvement is still a rarity. Radiologically, PBL appears as well circumscribed, heteroechoic, noncalcifying mass. Fine‐needle aspiration cytology (FNAC) is commonly used to diagnose this neoplasm; however, subcategorization requires immunophenotypic characterization of the neoplastic cells. Herein, we report two cases of PBL, including a HIV‐infected lady; in both the cases FNAC expressed features of non‐Hodgkin's lymphoma. Finally, immunohistochemistry on cell‐block with CD20 diagnosed both the cases as diffuse large B‐cell lymphoma (DLBCL). Diagn. Cytopathol. 2016;44:235–240. © 2015 Wiley Periodicals, Inc. 相似文献
8.
Adrenal Cysts: An Institutional Experience 总被引:1,自引:0,他引:1
Pradeep PV Mishra AK Aggarwal V Bhargav PR Gupta SK Agarwal A 《World journal of surgery》2006,30(10):1817-1820
Introduction Adrenal cysts are rare clinical entities. We report our institutional experience with adrenal cysts and also assess various
management options.
Material and methods Over the past 15 years the Department of Endocrine Surgery, Sanjay Gandhi Postgraduate Institute of Medical Sciences, Lucknow,
India, has had seven cases of adrenal cysts, of which two were functional: one patient had Cushing’s syndrome and the other
patient had pheochromocytoma. The other five cases were incidentally detected. Ultrasound scan and computerized tomography
(CT) scan were the imaging modalities. Four patients had a single cyst, two patients had two cysts, and one patient had multiple
unilateral cysts.
Results None of these cysts had foci of malignancy. Laparoscopic adrenalectomy was possible in three patients with no morbidity or
mortality.
Discussion The reported incidence in clinical series has been 5.4%. Pseudocysts, endothelial cysts, epithelial cysts, and hemorrhagic
cysts have been commonly described. The management can be conservative or surgical. It is generally agreed that a hormonal
work-up is necessary in all cases of adrenal cysts to rule out a sub-clinical disease. Adrenal neoplasms, including adrenocortical
carcinomas, can be associated with cysts that are benign in appearance. Percutaneous aspiration has been suggested as an alternative
treatment option if the cyst is not hormonally active and if there is no suspicion of malignancy. However, surgical excision
provides a definite histopathological diagnosis and also removes the fear of future complications such as hemorrhage into
the cyst and local pressure effects due to the tumor.
Conclusions Given that the adrenals are a vascular gland and taking into consideration the possibilities of bleeding and complications
in the cyst, our treatment of choice is the elective excision of adrenal cysts. 相似文献
9.
10.