Zaina S Inam

Conflicts of Interest The authors declare no conflicts of interest. Data Availability Statement For original data from the STAR registry, please contact Dr. Elizabeth Stenger, elizabeth.stenger@emory.edu. Supporting Information Filename Description ajh70200-sup-0001-Supinfo1.docxWord 2007 document , 138.4 KB Data S1: ajh70200-sup-0001-Supinfo1.docx. References 1 and , “Red Cell Transfusion and Alloimmunization in Sickle Cell Disease,” Haematologica 106, no.

Small bowel adenocarcinoma (SBA) is a rare cancer in the general population, but the incidence increases in patients with Lynch syndrome. The present case describes a 57-year-old white woman with a history of colon cancer status posthemicolectomy and diagnosis of Lynch syndrome. Twenty years after her operation, the patient presented with vague abdominal discomfort and constipation, and underwent an exploratory laparotomy which revealed a stage 3A SBA.

Sertoli-Leydig cell tumour (SLCT) is a rare, androgen-secreting sex cord–stromal tumour of the ovary that usually occurs in young premenopausal women. The major clinical manifestations are virilisation and defeminisation. The following case describes an 88-year-old G1P1 woman, 40 years after menopause, who presented with flushing, hirsutism, voice changes and alopecia along with significantly elevated levels of testosterone.