scholarly journals Intrahepatic Cholangiocarcinoma Skin Metastasis in a Patient with Hidradenitis Suppurativa: A Rare Entity

2020 ◽  
Vol 5 (1) ◽  
pp. 010-014
Author(s):  
Fakhreddine Ali Y ◽  
Yang Theresa ◽  
Liao Guanghong ◽  
Chavoshan Bahman
Keyword(s):  
Intrahepatic Cholangiocarcinoma ◽  
Hidradenitis Suppurativa ◽  
Skin Metastasis ◽  
Rare Entity

scholarly journals Skin Metastasis from Malignant Ovarian Tumor - A Rare Entity

2016 ◽  
Vol 33 (1) ◽  
pp. 41-43
Author(s):  
TS Chowdhury ◽  
U Ruman ◽  
TA Chowdhury
Keyword(s):  
Ovarian Cancer ◽  
Ovarian Carcinoma ◽  
Ovarian Tumor ◽  
Skin Metastasis ◽  
Ovarian Malignancy ◽  
Rare Entity ◽  
Malignant Ovarian Tumor ◽  
Previous Laparotomy ◽  
Skin Nodules ◽  
Serous Cyst

Skin metastasis from malignant ovarian carcinoma is rare and seen in only 3% of patients. Hence, we report a case of ovarian cancer with scar metastasis. The patient, a 31 year old woman presented with two skin nodules in the previous laparotomy scar which revealed metastatic papillary serous cyst adenocarcinoma on histopathology. So, it should be considered that ovarian malignancy is not always confined to pelvis and may present with associated skin lesion.J Bangladesh Coll Phys Surg 2015; 33(1): 41-43

scholarly journals Presentation of Intrahepatic Cholangiocarcinoma with Fulminant Hepatic Failure: A Case Report

2019 ◽  
Vol 02 (02) ◽  
pp. 135-139
Author(s):  
Thara Pratap ◽  
Muhammed Jasim Abdul Jalal ◽  
Pushpa Mahadevan ◽  
Abraham Koshy ◽  
Roy J. Mukkada ◽  
...  
Keyword(s):  
Case Report ◽  
Fulminant Hepatic Failure ◽  
Intrahepatic Cholangiocarcinoma ◽  
Hepatic Failure ◽  
Fatal Outcome ◽  
Final Diagnosis ◽  
Rare Entity ◽  
Cross Sectional ◽  
Cross Sectional Imaging ◽  
Sectional Imaging

AbstractFulminant hepatic failure as initial presentation due to diffuse parenchymal infiltration by cholangiocarcinoma is a rare entity. We present the case of a 49-year-old female patient who had a fatal outcome with acute liver failure due to diffuse intrahepatic cholangiocarcinoma. No definite mass lesion was identified on cross-sectional imaging. The final diagnosis was made on transjugular liver biopsy. This discussion highlights the possibility of infiltrative cholangiocarcinoma as a rare cause of fulminant hepatic failure.

Subcentimetric Incidental Intrahepatic Cholangiocarcinoma in an Explant Liver: Diagnostic Difficulty of a Rare Entity

2018 ◽  
Vol 26 (8) ◽  
pp. 739-744
Author(s):  
Suvradeep Mitra ◽  
Gude Geethanjali ◽  
Sahaj Rathi ◽  
Arunanshu Behera ◽  
Ashim Das
Keyword(s):  
Liver Disease ◽  
Autoimmune Hepatitis ◽  
Intrahepatic Cholangiocarcinoma ◽  
Poor Prognosis ◽  
Rare Case ◽  
Young Male ◽  
Advanced Stage ◽  
Rare Entity ◽  
Diagnostic Challenge ◽  
Neoplastic Lesion

Incidental intrahepatic cholangiocarcinoma (iCCA) is a rare neoplastic lesion in the explant liver specimens with an approximate incidence of 0.7%. The detection of iCCA is associated with poor prognosis in the posttransplant setting. The occurrence of a subcentimetric iCCA is very rare and poses a major diagnostic challenge to the pathologist. This article presents a rare case of subcentimetric iCCA in a young male in the background of advanced stage chronic liver disease resulting from autoimmune hepatitis possibly with chronic cholangiopathy along with the histomorphological differentials.

A carotid bifurcation pseudoaneurysm treated endovascularly in a patient with irradiated neck

VASA ◽  
2019 ◽  
Vol 48 (2) ◽  
pp. 193-195
Author(s):  
Christiana Anastasiadou ◽  
Chrisostomos Maltezos ◽  
George Galyfos ◽  
Sotirios Giannakakis ◽  
Nikos Zannes ◽  
...  
Keyword(s):  
Carotid Artery ◽  
Endovascular Treatment ◽  
Carotid Bifurcation ◽  
Rare Entity ◽  
Artery Pseudoaneurysm

Abstract. A carotid artery pseudoaneurysm in an irradiated neck is a rare entity with possible devastating results and management should be multidisciplinary. We present a successful endovascular treatment of a late carotid artery pseudoaneurysm following patch endarterectomy and cervical radiotherapy.

Castleman's Disease Masquerading as Sigmoid Colon Tumor and Hodgkin Lymphoma

Swiss Surgery ◽  
2002 ◽  
Vol 8 (1) ◽  
pp. 7-10 ◽  
Author(s):  
Altinli ◽  
Pekmezci ◽  
Balkan ◽  
Somay ◽  
M. Akif Buyukbese ◽  
...  
Keyword(s):  
Lymph Nodes ◽  
Hodgkin Lymphoma ◽  
Sigmoid Colon ◽  
Castleman’S Disease ◽  
Malignant Potential ◽  
Colon Tumor ◽  
Rare Entity ◽  
Castleman's Disease ◽  
Mediastinal Lymph Nodes ◽  
Histologic Types

Castleman's disease is a benign lymphoid neoplasm first reported as hyperplasia of mediastinal lymph nodes. Some authors referred to the lesions as isolated tumors, described as a variant of Hodgkin's disease with a possibility of a malignant potential and others proposed that the lymphoid masses were of a hamartomatous nature. Three histologic variants and two clinical types of the disease have been described. The disease may occur in almost any area in which lymph nodes are normally found. The most common locations are thorax (63%), abdomen (11%) and axilla (4%). We report two separate histologic types of Castleman's disease which were rare in the literature, mimicking sigmoid colon tumor and Hodgkin lymphoma. The diagnostic and therapeutic aspects of this rare entity is discussed.

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