Kurimoto Miwa, Sonoki Takashi, Nakamura Yasushi, Yamamoto Yasuhide, Maeda Yoshimasa, Kuriyama Kodai, Mushino Toshiki, Hosoi Hiroki, Murata Shogo, Shimanuki Masaya, Hatanaka Kazuo, Hanaoka Nobuyoshi, Kato Jun, Nakakuma Hideki
Department of Hematology/Oncology, Wakayama Medical University, Japan.
Intern Med. 2014;53(6):581-5. doi: 10.2169/internalmedicine.53.1625.
A 57-year-old Japanese man was admitted to our hospital with diarrhea, weight loss and malabsorption. Due to a high serum IgA level, we suspected α-heavy chain disease (α-HCD). However, no monoclonal IgA was detected on protein electrophoresis or immunofixation. Immunohistochemical staining of intestinal biopsy specimens showed proliferation of CD138(+)IgA(+) cells, compatible with a diagnosis of α-HCD. Most α-HCD patients exhibit M-proteins in the serum on electrophoresis or immunoelectrophoresis; however, some patients lack detectable M-proteins, similar to our patient. Therefore, when α-HCD is suspected based on the clinical features, immunohistochemistry is required to make a diagnosis.