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Table 2 Characteristics of five reported DI-MDS cases and the presented two cases

From: Myelodysplastic syndrome presenting with central diabetes insipidus is associated with monosomy 7, visible or hidden: report of two cases and literature review

Reference

Age (years)

MDS subtype

Partial/complete deletion of chromosome 7

MRI abnormal

Treatment of MDS

Outcome of CDI

Time to AML (months)

OS (months)

Case 1

43

RAEB1

Yes

A slightly thickened pituitary stalk and a small nodule in the left pituitary

Allo-HCT

Controlled by desmopressin and cured after HCT

No

13 +

Case 2

40

RAEB1

Yes

No

Decitabine and Allo-HCT

Controlled by desmopressin and HCT, reappeared when disease progress

2

11

4

74

RAEB 1

Yes

No

Supportive care

Controlled by desmopressin

2

2

6

6

RAEB 1

Yes

No

Allo-HCT

Controlled by desmopressin and cured after HCT

No

NA

7

53

RAEB 2

No (Norma karyotype)

Nodular lesion on pituitary stalk & absent of posterior “bright spot” of neurohypophysis on T1-weighed MRI

Chemotherapy and Allo-HCT

Controlled by desmopressin and need for desmopressin persists after allo-HCT

No

18 +

9

60

MDS-MLD

No (Norma karyotype)

Attenuation of “bright spot”

Chemotherapy

Recovered after chemotherapy

1

NA

10

73

NA

Yes

Absent of posterior “bright spot” & symmetrical enhancing lesions in the hypothalamus

NA

Temporary controlled by desmopressin

3

3

  1. MDS myelodysplastic syndrome, CDI central diabetes insipidus, MRI magnetic resonance imaging, NA not available, AML acute myeloid leukemia, OS overall survival, RAEB refractory anemia with excess blasts, Allo-HCT allogeneic hematopoietic cell transplant, MDS-MLD MDS with multilineage dysplasia