scholarly journals Isolated myeloid sarcoma causing obstructive jaundice in duodenal ampulla: a very rare case

2020 ◽  
Vol 42 ◽  
pp. 17
Author(s):  
Ömer Ekinci ◽  
Mustafa Merter ◽  
Mehmet Aslan ◽  
İlknur Calık
Keyword(s):  
Obstructive Jaundice ◽  
Rare Case ◽  
Myeloid Sarcoma

scholarly journals Isolated myeloid sarcoma of lumbar spine without bone marrow involvement: a rare case report and treatment dilemma

2021 ◽  
Vol 0 ◽  
pp. 0-0
Author(s):  
Janpreet S. Bhandohal ◽  
Leila Moosavi ◽  
Igor Garcia-Pacheco ◽  
Gian Yakoub ◽  
Rahul D. Polineni ◽  
...  
Keyword(s):  
Bone Marrow ◽  
Case Report ◽  
Lumbar Spine ◽  
Rare Case ◽  
Bone Marrow Involvement ◽  
Myeloid Sarcoma ◽  
Rare Case Report

scholarly journals A rare case of Gingival Myeloid sarcoma in a child

2017 ◽  
Vol 7 (2) ◽  
pp. 1227-1230
Author(s):  
Meghashree Vishwanath ◽  
Purnima S Rao ◽  
Muktha R Pai
Keyword(s):  
Lymph Node ◽  
Rare Case ◽  
Soft Tissues ◽  
Myeloid Cells ◽  
Myeloid Sarcoma ◽  
Rare Tumour ◽  
Immature Myeloid Cells

Myeloid sarcoma is a rare tumour composed of immature myeloid cells. Its occurrence in childhood is rare. Only a few cases of intraoral myeloid sarcoma have been reported in literature. We present a case of myeloid sarcoma with simultaneous involvement of intraoral soft tissues and lymph node. Here, importance is given to suspect this frequently misdiagnosed disease. 

Mucin-filled CBD, difficult to manage cholangitis

2021 ◽  
Vol 14 (1) ◽  
pp. e238363
Author(s):  
Manish Kumar ◽  
Ujjwal Sonika ◽  
Sanjeev Sachdeva ◽  
Ashok Dalal
Keyword(s):  
Bile Duct ◽  
Common Bile Duct ◽  
Obstructive Jaundice ◽  
Rare Case ◽  
Malignant Potential ◽  
Cystic Neoplasm ◽  
Stricture Formation ◽  
Intraductal Papillary Mucinous Neoplasms ◽  
Mucinous Neoplasms ◽  
Optimum Management

Intraductal papillary mucinous neoplasms (IPMNs) are mucin-secreting cystic neoplasm of pancreas. They have a malignant potential. They are usually localised to the pancreas but occasionally can involve surrounding structures (1.9%–6.6%), like bile duct and duodenum, and are labelled as IPMN with invasion. Jaundice as a manifestation of IPMN is not common (4.5%). It can present as jaundice as a result of invasion of common bile duct (CBD) resulting in stricture formation or uncommonly as a result of fistulising to CBD with resultant obstruction of CBD by thick mucin secreted by this tumour. As only few cases (around 23) of mucin-filled CBD are reported in the literature. We are presenting our experience in dealing a rare case of obstructive jaundice caused by IPMN fistulising into CBD, highlighting the difficulties faced in managing such case, especially with regards to biliary drainage and what can be the optimum management in such cases.

scholarly journals Extramedullary Monoblastic Sarcoma/Myeloid Sarcoma of Paraspinal Region Without Myeloid Leukemia: A Rare Case Report

2018 ◽  
Vol 150 (suppl_1) ◽  
pp. S49-S50
Author(s):  
Mitul Modi ◽  
Vipulkumar Prajapati ◽  
Irappa Madabhavi ◽  
Himanshu Kavani ◽  
Mansi Shah
Keyword(s):  
Case Report ◽  
Myeloid Leukemia ◽  
Rare Case ◽  
Myeloid Sarcoma ◽  
Rare Case Report

Myeloid sarcoma of the extrahepatic bile ducts presenting as obstructive jaundice.

Apmis ◽  
2006 ◽  
Vol 114 (9) ◽  
pp. 666-668 ◽  
Author(s):  
M. CARMEN GONZÁLEZ-VELA ◽  
J. FERNANDO VAL-BERNAL ◽  
MARTA MAYORGA ◽  
M. LUISA CAGIGAL ◽  
FIDEL FERNÁNDEZ ◽  
...  
Keyword(s):  
Obstructive Jaundice ◽  
Bile Ducts ◽  
Myeloid Sarcoma ◽  
Extrahepatic Bile Ducts

scholarly journals A Rare Case of Myeloid Sarcoma Presenting as an Anorectal Ulcer

2012 ◽  
Vol 2012 ◽  
pp. 1-5 ◽  
Author(s):  
Laxmi Parsa ◽  
Priti Bijpuria ◽  
Daniel Ringold ◽  
David Stein
Keyword(s):  
Immunohistochemical Staining ◽  
Myeloid Leukemia ◽  
Rare Case ◽  
Soft Tissues ◽  
Histochemical Staining ◽  
Myeloid Sarcoma ◽  
Atypical Presentation ◽  
Rare Tumor ◽  
Gastrointestinal Complaint ◽  
Acute Myeloid

Myeloid Sarcoma is a rare tumor composed of myeloblasts occurring at an extramedullary site like bones, or various soft tissues. Myeloid sarcoma may involve the gastrointestinal tract very rarely either solitarily, or occurring simultaneously with acute myeloid leukemia. Its diagnosis is challenging and needs biopsy and immunohistochemical staining. We are describing a case of myeloid sarcoma which presented as a painful anal ulcer mimicking an atypical fissure. Its appearance resembled crohn’s disease on sigmoidoscopy. A biopsy of the ulcer along with histochemical staining led to the diagnosis of myeloid sarcoma. Our case demonstrates the need for aggressive evaluation of any common gastrointestinal complaint with an atypical presentation.

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