scholarly journals The Enigmatic Kikuchi-Fujimoto Disease: A Case Report and Review

2014 ◽  
Vol 2014 ◽  
pp. 1-4 ◽  
Author(s):  
Hassan Tariq ◽  
Vinaya Gaduputi ◽  
Arsalan Rafiq ◽  
Roopalekha Shenoy

We report this case of a 33-year-old African American woman who presented to the clinic with preauricular and submandibular masses that she had noticed 6 weeks earlier. She gave a remote history of noticing bilateral cervical masses 3 years prior to this presentation that had not been investigated at the time and resolved spontaneously. Excisional biopsies of the cervical lymph nodes showed morphologic and immunophenotypic findings suggestive of Kikuchi Fujimoto disease (KFD). KFD is an uncommon, self-limited, and perhaps an underdiagnosed entity with an excellent prognosis. It mimics malignant lymphoma in presentation and therefore an accurate clinicopathological differentiation is crucial.

2015 ◽  
Vol 2015 ◽  
pp. 1-6 ◽  
Author(s):  
Mark Ashamalla ◽  
Marita S. Teng ◽  
Joshua Brody ◽  
Elizabeth Demicco ◽  
Rahul Parikh ◽  
...  

We are reporting a case of a 62-year-old African American woman with a history of gastric MALT lymphoma successfully treated with radiation who presented with a laryngeal MALT lymphoma 4 years after her original diagnosis. She received definitive radiation with a complete response. The case presented is unique for the rare presentation of a MALT lymphoma in the larynx, especially in light of the patient’s previously treated gastric MALT lymphoma years ago.


F1000Research ◽  
2014 ◽  
Vol 3 ◽  
pp. 297 ◽  
Author(s):  
Rohit Kumar Gudepu ◽  
Mohtashim A. Qureshi ◽  
Ihtesham A. Qureshi ◽  
Lakshman Rao

Moyamoya is a rare idiopathic progressive vaso-occlusive disease characterized by irreversible condition of main blood vessels to the brain as they enter into the skull. We present a case of 36 year old African American female presenting to the Out Patient Clinic with headache which were on and off for 4-6 months and did not relieve on routine medical therapy. It was associated with weakness on right side for last few days. The patient was investigated with CT Angiogram, diagnosed as Moyamoya disease and operated. She has been followed up for the last 5 years and the patient has not complained of any headaches or focal neurological symptoms.


2018 ◽  
Vol 5 (3) ◽  
pp. 17
Author(s):  
Jerad A.K. Harris ◽  
Mark Shane Gillispie ◽  
Claribel Solario ◽  
Melody L. Tran ◽  
Rogelio Pinon-Gutierrez ◽  
...  

We describe a 47-year-old African American woman affected by a rapidly progressing thromboangiitis associated with high serum levels of lipoprotein(a) (Lp(a)).


Genealogy ◽  
2020 ◽  
Vol 4 (2) ◽  
pp. 49 ◽  
Author(s):  
Traci Wilson-Kleekamp

This paper deploys narrative inquiry and analysis to capture the oral history of two families’ intergenerational memory of an African American woman named Celia who was hanged in 1855 for killing her owner Robert Newsom. It is the first scholarly investigation into the intergenerational memory of both black and white descendants of Robert Newsom, and the first to be conducted utilizing the theory of critical family history. Through the paradigm of Black Feminist Thought, the paper analyzes the power imbalances embedded in the narrative about family relations, especially those that conjure race, gender roles and class produced through oral history.


2017 ◽  
Vol 26 (4) ◽  
pp. 353-355 ◽  
Author(s):  
Osama Elfituri ◽  
Snehal Sonawane ◽  
Haoliang Xu ◽  
Michael A. Warso ◽  
Elizabeth Wiley

Mammary sclerosing lobular hyperplasia is an uncommon benign fibroproliferative lesion of adolescent and young women, often of African American heritage with an incidence of ~3%. Patients generally complain of a palpable, painless, or slightly tender and well-defined lump in breast. Very rarely, this lesion may be bilateral and diffuse. The definitive diagnosis of sclerosing lobular hyperplasia requires histopathologic evaluation. Here, we describe a case of diffuse sclerosing lobular hyperplasia in a 29-year-old African American woman that required bilateral mastectomy and recurred bilaterally requiring second resections. This appears to be the first report of this phenomenon.


Author(s):  
Soyica Colbert

Born in Chicago in 1930, Lorraine Hansberry made history when her play A Raisin in the Sun premièred on Broadway in 1959 as the first work by an African-American woman to appear on the Great White Way. Realist in style, A Raisin in the Sun engaged with modern American drama’s investigation of the salience of the American Dream in the context of the Cold War, situating the deferred dreaming of the Younger family within a long history of foreclosed desire and possibility. Hansberry remains best-known for A Raisin in the Sun, but the play both exemplifies and overshadows her other accomplishments as a black lesbian artist-activist, only gesturing toward the expansive political vision of her work as a whole, including her exploration of slavery in The Drinking Gourd (1960), her treatment of apocalypse in What Use Are Flowers (1962), and her consideration of black freedom movements in Les Blancs (1964) and The Movement: A Documentary of a Struggle for Equality (1964).


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