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1. 赤血球増加症患者に対する診断的アプローチdiagnostic approach to the patient with polycythemia [show details]
…of rare syndromes caused by inherited (germline) mutations . Examples include primary familial and congenital polycythemia, which may be caused by an activating mutation of the EPO-receptor (EPOR) or other…
2. 先天性赤血球増多症および真性多血症の分子学的病因molecular pathogenesis of congenital polycythemic disorders and polycythemia vera [show details]
…very low in familial 2,3-BPG deficiency. Primary familial and congenital polycythemia (PFCP, also called benign erythrocytosis and autosomal dominant erythrocytosis) is an uncommon cause of polycythemia but …
3. 性腺機能低下を呈する男性に対するテストステロン治療testosterone treatment of male hypogonadism [show details]
4. テストステロン低下症の高齢男性へのアプローチapproach to older men with low testosterone [show details]
5. ヘモグロビンの酸素親和性に関する遺伝性疾患genetic disorders of hemoglobin oxygen affinity [show details]

English Journal

The role of F-FDG PET in the assessment of a benign hematological disorder: polycythemia.

Ayubcha C, Hosoya H, Seraj SM, Zadeh MZ, Werner T, Alavi A.
Hellenic journal of nuclear medicine. ;22(1)4-5.
Fluorine-18 fluorodeoxyglucose positron emission tomography (F-FDG PET) imaging was conceived in the early 1970 by investigators at the University of Pennsylvania as a research technique to measure brain metabolism and function by employing a non-invasive imaging approach. Soon after the introductio
PMID 30843002

The first case of neonatal priapism during hypothermia for hypoxic-ischemic encephalopathy and a literature review.

Fanni C, Marcialis MA, Pintus MC, Loddo C, Fanos V.
Italian journal of pediatrics. 2018 Jul;44(1)85.
Neonatal priapism is a rare condition with only 26 described cases in literature since 1879. It is defined as a persistent penile erection occurring in the first 28 days of life, lasting at least 4 h that usually happens in the first days (from 2 to 12 days). It is a very different condition comp
PMID 30053817

Rocha GM, Flor-De-Lima FS, Guimaraes HA.
Minerva pediatrica. 2018 Jun;70(3)217-224.
Grunting respirations occurring in the first hours of life is a frequent nonspecific clinical sign. Our objective was to assess the clinical significance of grunting lasting over two hours of birth in term and near term newborns. A five years retrospective study of all newborns ≥35+0 weeks of gest
PMID 27607482

Differential Diagnoses of Macrocytic Anemia, Reticulocytosis and Low Serum Haptoglobin in Patients with Myelodysplastic Syndromes/Acute Leukemia: Comment on "Two Cases of Acute Erythroid Leukemia Presenting with Marked Macrocytic Anemia, Reticulocytosis and Hemolysis"

Truncated erythropoietin receptor causes dominantly inherited benign human erythrocytosis

佐藤雄一,真栄田篤彦,横山〓
臨床血液 21(8), 1201-1208, 1980
… A 10-year-old girl with erythrocytosis is reported. … Erythrocytosis was noticed at the age of ten when she first visited the outpatient clinic of the Pediatric Department of Hirosaki University because of upper respiratory infection. … Although there was no evidence of erythrocytosis in the family, the findings in this patient appear to be those of a condition which has been called benign familial erythrocytosis. …
NAID 130004498259