TY - JOUR
T1 - A rare case of isolated splenic sarcoidosis
T2 - A case report and literature review
AU - Kobayashi, Kazuki
AU - Einama, Takahiro
AU - Fujinuma, Ibuki
AU - Tsunenari, Takazumi
AU - Miyata, Yoichi
AU - Iwasaki, Toshimitsu
AU - Asakuma, Junichi
AU - Soga, Shigeyoshi
AU - Shinmoto, Hiroshi
AU - Tsujimoto, Hironori
AU - Hase, Kazuo
AU - Ueno, Hideki
AU - Kishi, Yoji
N1 - Publisher Copyright:
© 2021, Spandidos Publications. All rights reserved.
PY - 2021/2
Y1 - 2021/2
N2 - Sarcoidosis is a multisystemic granulomatous disease. It is rarely isolated in the spleen. The present report describes a case of isolated splenic sarcoidosis that was diagnosed histologically following laparoscopic splenectomy. A 76-year-old woman, who underwent radical nephroureterectomy 7 years earlier for left renal pelvic cancer and mastectomy 6 years earlier for left breast cancer in another facility, was referred to our hospital for assessment of splenic tumors that were identified during a follow-up examination. The computed tomography scans revealed multiple nodules in the spleen, which had increased in size over 2 years. Positron emission tomography revealed accumulation of [18F]-fluorodeoxyglucose in the spleen. Laparoscopic splenectomy was performed and the diagnosis of sarcoidosis was confirmed histologically. A review of previous reports and the present case suggested that diagnosis of splenic sarcoidosis should be considered when the CT scans show multinodular splenic tumors, and sarcoidosis might be associated with malignant tumors.
AB - Sarcoidosis is a multisystemic granulomatous disease. It is rarely isolated in the spleen. The present report describes a case of isolated splenic sarcoidosis that was diagnosed histologically following laparoscopic splenectomy. A 76-year-old woman, who underwent radical nephroureterectomy 7 years earlier for left renal pelvic cancer and mastectomy 6 years earlier for left breast cancer in another facility, was referred to our hospital for assessment of splenic tumors that were identified during a follow-up examination. The computed tomography scans revealed multiple nodules in the spleen, which had increased in size over 2 years. Positron emission tomography revealed accumulation of [18F]-fluorodeoxyglucose in the spleen. Laparoscopic splenectomy was performed and the diagnosis of sarcoidosis was confirmed histologically. A review of previous reports and the present case suggested that diagnosis of splenic sarcoidosis should be considered when the CT scans show multinodular splenic tumors, and sarcoidosis might be associated with malignant tumors.
KW - Isolated splenic sarcoidosis
KW - Multinodular splenic tumors
KW - Sarcoidosis
UR - http://www.scopus.com/inward/record.url?scp=85099132361&partnerID=8YFLogxK
UR - http://www.scopus.com/inward/citedby.url?scp=85099132361&partnerID=8YFLogxK
U2 - 10.3892/mco.2020.2184
DO - 10.3892/mco.2020.2184
M3 - Review article
AN - SCOPUS:85099132361
SN - 2049-9450
VL - 14
SP - 1
EP - 5
JO - Molecular and Clinical Oncology
JF - Molecular and Clinical Oncology
IS - 2
M1 - 22
ER -