scholarly journals Pachydermodactyly: A Rare Type of Macrodactyly as a Dermatological Sign of Compulsive Behavior and Repetitive Minor Trauma; a Case Report and Review of the Literature

2018 ◽  
Vol 20 (9) ◽  
Author(s):  
Ivana Kavecan ◽  
Milos Pajic ◽  
Nada Vuckovic ◽  
Tatjana Redzek Mudrinic ◽  
Artur Bjelica ◽  
...  
2021 ◽  
pp. 1071-1079
Author(s):  
Jennifer Y. Ge ◽  
Beth Overmoyer

Inflammatory breast cancer (IBC) is a rare type of breast cancer that is associated with poor outcomes compared with non-IBC. Overexpression of HER2 is enriched in IBC, and those with HER2-positive disease have a relatively favorable prognosis, with improved survival over the last two decades driven by the advent of novel targeted therapies. Here, we present two patients who have survived for over 10 years after being diagnosed with de novo metastatic HER2-positive IBC. We review the data for the treatments available for metastatic HER2-positive IBC and the evolving treatment recommendations for this disease.


2016 ◽  
Vol 8 (1) ◽  
pp. 66-68
Author(s):  
Thankam Varma ◽  
Shashidhar Boraiah

ABSTRACT Cesarean scar ectopic pregnancy is becoming increasingly common in tertiary care hospitals. Cesarean scar pregnancy is a rare type of ectopic pregnancy associated with complications, such as uterine rupture, uncontrollable bleeding which may lead to hysterectomy and increased maternal morbidity and mortality and subsequent infertility. Options available for treatment, such as dilatation and curettage, excision of trophoblastic tissues using laparotomy or laparoscopy, systemically administered methotrexate, and more recently uterine artery embolization. We report two such cases between 2012 and 2013 managed conservatively. How to cite this article Boraiah S, Varma T, Shankar K. Cesarean Scar Ectopic Pregnancy: Case Report and Review of the Literature. J South Asian Feder Obst Gynae 2016;8(1):66-68.


2020 ◽  
Vol 48 (01) ◽  
pp. 061-065
Author(s):  
Margarida Areias Marques Miranda ◽  
Pedro Mota ◽  
Pedro Cardoso ◽  
Alexandre Pereira ◽  
Vânia Oliveira

AbstractMerkel Cell Carcinoma is a rare type of aggressive and often fatal neuroendocrine tumor of the skin.We report a clinical case of a 56-year-old female with a Merkel cell carcinoma on the left hand, without distant metastasis, treated with surgical excision of the lesion and radiotherapy.Based on this clinical case a research and review of the literature on this rare neoplasia was carried out.


2019 ◽  
Vol 2 (2) ◽  
pp. 44-47
Author(s):  
Mokrani A ◽  
Behi K ◽  
Sbika W ◽  
Mghirbi F ◽  
Yahyoui Y ◽  
...  

Hepatoid adenocarcinoma (HAC) is defined as an extrahepatic tumor with hepatocyte differentiation. Hepatoid adenocarcinoma of the stomach (HAS) is a rare type of gastric cancer characterized by unique clinico-pathological features and a poor prognosis. We report a case of a metastatic HAS with a review of the literature.


Author(s):  
Emmanuel Ekanem ◽  
Santosh Poozhikalayil ◽  
Anita Sinha

The Bombay blood group is a rare type of blood group which is very distinct from the ABO system and was first discovered in India about five decades ago. This blood group describes individuals who lack the H antigen and thus present with the anti H antibodies in addition to anti A and anti B antibodies. Bombay blood group is sometimes mistaken for blood group O. The significance of this blood group is in its ability to potentially cause fatal blood transfusion reaction and haemolytic disease of the foetus and the neonate. Aim: This case report aims to elucidate the rare occurrence of the Bombay blood group. Methods: We describe a case report of the pregnancy, labour and delivery of a multiparous Indian woman with the Bombay blood group in her second pregnancy. Results: The index case had an uneventful pregnancy, labour and delivery without the need for blood transfusion. The neonate was Rhesus D positive and did not have any complications. Conclusion: Bombay blood group is a rare blood group which can lead to blood transfusion reactions and haemolytic disease of the foetus and newborn. Pregnancy, labour and delivery should be managed in a unit with the availability of anti H blood to avoid foetal and maternal complications.


2015 ◽  
Vol 134 (1) ◽  
pp. 84-87 ◽  
Author(s):  
Everton Cazzo ◽  
Helena Paes de Almeida de Saito

CONTEXT: Gastric stump cancer after gastric resection is a well-known disease. It may be a newly developed cancer after resection due to benign disease, or recurrent or residual disease after oncological surgery. The predominant histological type is usually adenocarcinoma. This study aimed to report on a rare occurrence of a mixed adenoneuroendocrine carcinoma (MANEC) on the gastric stump. CASE REPORT: The case of an 83-year-old female who presented a locally aggressive gastric stump MANEC, 35 years after Billroth II gastrectomy to treat a peptic ulcer, is reported. The patient underwent resection and adjuvant therapy. She has been followed up for one year without signs of recurrence. CONCLUSION: MANEC is a rare type of gastrointestinal neoplasm. The classification, histopathology, clinical features, treatment issues and prognosis are discussed along with a brief review of the literature.


2000 ◽  
Vol 35 (7) ◽  
pp. 1117-1119 ◽  
Author(s):  
Donald C. Liu ◽  
Jaime A. Rodriguez ◽  
Funda Meric ◽  
James L. Geiger

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