Sarcomatoid carcinoma of the small intestine: Histologic, immunohistochemical and ultrastructural features of three cases and its differential diagnosis

1996 ◽  
Vol 46 (9) ◽  
pp. 682-688 ◽  
Author(s):  
Takeaki Fukuda ◽  
Tomoko Kamishima ◽  
Yoshihisa Ohnishi ◽  
Toshimitsu Suzuki
2001 ◽  
Vol 87 (6) ◽  
pp. 431-435 ◽  
Author(s):  
Dolores Di Vizio ◽  
Luigi Insabato ◽  
Giovanni Conzo ◽  
Brian T Zafonte ◽  
Gerardo Ferrara ◽  
...  

Sarcomatoid carcinoma (SC) is a well defined tumor type that may occur in all organs and anatomic sites but most commonly in the head1, neck1, respiratory tract2-4, breast5, and genitourinary tract6-11. It is a biphasic tumor showing both epithelial- and mesenchymal-like differentiation; however, its carcinomatous nature is widely recognized12. SC is rare in the gastrointestinal tract. In the esophagus it accounts for less than 5% of all malignancies12-16 and approximately only 35 cases have been described in the stomach12,17-18. Very few cases have been observed in the small intestine19-20, anorectal junction21, liver22, and pancreas23-24. To our knowledge only eight cases of SC have been reported in the colon25-32. We report a case of primary colonic SC. Both morphological and immunohistochemical analyses are provided along with an evaluation of the unusual clinical history, therapeutic implications, and controversial differential diagnosis.


2013 ◽  
Vol 2013 ◽  
pp. 1-3 ◽  
Author(s):  
Sarah Alghamdi ◽  
Yumna Omarzai

Malignant melanoma of the gastrointestinal tract is an uncommon neoplasm that could be primary or metastatic. Small intestine represents the most common site for the metastatic melanoma; however, it could be found anywhere in the gastrointestinal tract. Intussusception is a rare cause of intestinal obstruction in adults compared to children. In 90% of the cases, the underlying cause can be found, and in 65% of the cases, intussusception is caused by the neoplastic process. The majority of the neoplasms are benign, and about 15% are malignant. Metastatic melanoma is one of the most common metastatic malignancies to the gastrointestinal tract; however, the premortem diagnosis is rarely made. Here, we report an uncommon clinical presentation of metastatic melanoma causing intussusception in an 80-year-old man. This diagnosis should be considered in a differential diagnosis in any patient who presents with gastrointestinal symptoms and a history of melanoma.


2012 ◽  
Vol 02 (01) ◽  
pp. 45-47
Author(s):  
Shetty K. Padma ◽  
Harish S. Permi ◽  
C.N. Patil ◽  
Michelle Mathias

AbstractSarcomatoid carcinoma occurring in the small intestine is very rare. They can be monophasic or biphasic. We report a rare case of monophasic Sarcomatoid carcinoma of the small intestine in a 60 year old male patient. The tumor was an ulceronodular mass involving the ileum circumferentially. The tumor infiltrated the full thickness of the intestinal wall and the serosa of an adjacent loop of ileum. Microscopically, the tumor was composed of sheets of malignant spindle cells. The carcinomatous nature of the tumor was evident only after Immunohistochemistry. The diagnosis of sarcomatoid carcinoma should be considered in the differential diagnosis of malignant spindle cell tumor of small intestine and immunohistochemical stains are required for the correct diagnosis.


2021 ◽  
Vol 57 (1) ◽  
pp. 89
Author(s):  
Nurwahyuna Rosli ◽  
Nordashima Abd Shukor

1986 ◽  
Vol 67 (6) ◽  
pp. 441-444
Author(s):  
R. F. Akberov

Functional disorders of the gastrointestinal tract in young children are the most difficult and insufficiently studied issues of clinical medicine. So far, such relevant issues as the mechanism of regurgitation and vomiting, the origin of pylorostenosis and dyskinetic disorders of the small intestine have not been elucidated. Unified methods of diagnosis and differential diagnosis of both functional and organic changes of the gastrointestinal tract, especially in children in the first days of life, have not been developed.


1989 ◽  
Vol 20 (9) ◽  
pp. 858-863 ◽  
Author(s):  
Susan S. Robey-Cafferty ◽  
Elvio G. Silva ◽  
Karen R. Cleary

1996 ◽  
Vol 66 (9) ◽  
pp. 636-639 ◽  
Author(s):  
K. Y. Lam ◽  
C. Y. Leung ◽  
J. W. C. Ho

2005 ◽  
Vol 96 (6) ◽  
pp. 640-643
Author(s):  
Takako Masue ◽  
Mitsuhiro Taniguchi ◽  
Toshimi Takeuchi ◽  
Shunsuke Sakai

2009 ◽  
Vol 33 (5) ◽  
pp. 413
Author(s):  
S. Romano ◽  
A. Russo ◽  
S. Daniele ◽  
G. Tortora ◽  
F. Maisto ◽  
...  

2014 ◽  
Vol 138 (10) ◽  
pp. 1272-1277 ◽  
Author(s):  
Megan Alderman ◽  
Lakshmi P. Kunju

We illustrate a case of an inflammatory myofibroblastic tumor (IMT) involving the bladder in a woman with dysuria and review the literature and differential diagnosis. Inflammatory myofibroblastic tumor, also referred to as pseudosarcomatous myofibroblastic proliferation, is a rare lesion that can arise in the genitourinary system and is characterized by a fascicular arrangement of myofibroblasts with admixed inflammatory cells and slitlike vessels. Urinary bladder IMT can be a diagnostic pitfall because its histologic features (brisk mitoses, invasion into muscularis propria, and prominent nucleoli) can mimic malignancy. The differential diagnosis of urinary bladder IMT includes sarcomatoid carcinoma and leiomyosarcoma. Diagnostic features such as bland nuclear chromatin, ganglion-like cells, pale eosinophilic cytoplasm with long processes, overexpression of anaplastic lymphoma kinase (immunohistochemistry or gene rearrangement studies), and the absence of atypical mitoses help distinguish IMT from its malignant mimics. Current controversies regarding postoperative spindle cell nodule and IMT are discussed.


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