Pancytopenia

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Abdul Hamid Zargar - One of the best experts on this subject based on the ideXlab platform.

  • Hematological response of Pancytopenia to glucocorticoids in patients with Sheehan’s syndrome
    Pituitary, 2012
    Co-Authors: Bashir Ahmad Laway, Javid Rasool Bhat, Mohd Iqbal Lone, Jeelani Samoon, Abdul Hamid Zargar
    Abstract:

    Sheehan’s syndrome presents with panhypopituitarism after childbirth, usually preceded by post partum hemorrhage. Hematological abnormalities like Pancytopenia with hypocellular marrow in these patients are reported rarely. Though multiple hormone deficiencies may contribute to Pancytopenia in Sheehan’s syndrome, complete recovery is observed after achieving eucortisolemic and euthyroid state. The predominant role of thyroxine or glucocorticoids in reversing Pancytopenia in these patients has not been studied. We present the clinical, hormonal, hematological course and response to glucocorticoids in a patient of Sheehan’s syndrome presenting with Pancytopenia. Complete recovery of Pancytopenia was observed after achieving eucortisolemic state thus concluding that gulcocorticoid replacement is sufficient to reverse Pancytopenia in these patients.

  • Sheehan’s syndrome with Pancytopenia—complete recovery after hormone replacement (case series with review)
    Annals of Hematology, 2010
    Co-Authors: Bashir Ahmad Laway, Javid Rasool Bhat, Mohd Iqbal Lone, Shahnaz Ahmad Mir, Raja Sultan Zaman Khan, Abdul Hamid Zargar
    Abstract:

    Reports of Pancytopenia in patients with Sheehan’s syndrome are rare, because the disorder is not commonly seen in western countries. A case series of Pancytopenia in three patients of Sheehan’s syndrome is presented. Three women aged 22, 30, and 34 years developed Sheehan’s syndrome preceded by post partum hemorrhage. During investigations, they were found to have Pancytopenia with hypocellular marrow. Treatment with thyroxine and glucocorticoids resulted in complete recovery after attaining euthyroid and eucortisolemic state. Review of literature revealed the rarity of the disorder, with only four cases reported so far. Multiple anterior pituitary hormone deficiencies in Sheehan’s syndrome are responsible for Pancytopenia; replacement of thyroid and cortisol hormones results in complete recovery.

  • sheehan s syndrome with Pancytopenia complete recovery after hormone replacement case series with review
    Annals of Hematology, 2010
    Co-Authors: Bashir Ahmad Laway, Javid Rasool Bhat, Mohd Iqbal Lone, Shahnaz Ahmad Mir, Raja Sultan Zaman Khan, Abdul Hamid Zargar
    Abstract:

    Reports of Pancytopenia in patients with Sheehan’s syndrome are rare, because the disorder is not commonly seen in western countries. A case series of Pancytopenia in three patients of Sheehan’s syndrome is presented. Three women aged 22, 30, and 34 years developed Sheehan’s syndrome preceded by post partum hemorrhage. During investigations, they were found to have Pancytopenia with hypocellular marrow. Treatment with thyroxine and glucocorticoids resulted in complete recovery after attaining euthyroid and eucortisolemic state. Review of literature revealed the rarity of the disorder, with only four cases reported so far. Multiple anterior pituitary hormone deficiencies in Sheehan’s syndrome are responsible for Pancytopenia; replacement of thyroid and cortisol hormones results in complete recovery.

Bashir Ahmad Laway - One of the best experts on this subject based on the ideXlab platform.

  • Hematological response of Pancytopenia to glucocorticoids in patients with Sheehan’s syndrome
    Pituitary, 2012
    Co-Authors: Bashir Ahmad Laway, Javid Rasool Bhat, Mohd Iqbal Lone, Jeelani Samoon, Abdul Hamid Zargar
    Abstract:

    Sheehan’s syndrome presents with panhypopituitarism after childbirth, usually preceded by post partum hemorrhage. Hematological abnormalities like Pancytopenia with hypocellular marrow in these patients are reported rarely. Though multiple hormone deficiencies may contribute to Pancytopenia in Sheehan’s syndrome, complete recovery is observed after achieving eucortisolemic and euthyroid state. The predominant role of thyroxine or glucocorticoids in reversing Pancytopenia in these patients has not been studied. We present the clinical, hormonal, hematological course and response to glucocorticoids in a patient of Sheehan’s syndrome presenting with Pancytopenia. Complete recovery of Pancytopenia was observed after achieving eucortisolemic state thus concluding that gulcocorticoid replacement is sufficient to reverse Pancytopenia in these patients.

  • Sheehan’s syndrome with Pancytopenia—complete recovery after hormone replacement (case series with review)
    Annals of Hematology, 2010
    Co-Authors: Bashir Ahmad Laway, Javid Rasool Bhat, Mohd Iqbal Lone, Shahnaz Ahmad Mir, Raja Sultan Zaman Khan, Abdul Hamid Zargar
    Abstract:

    Reports of Pancytopenia in patients with Sheehan’s syndrome are rare, because the disorder is not commonly seen in western countries. A case series of Pancytopenia in three patients of Sheehan’s syndrome is presented. Three women aged 22, 30, and 34 years developed Sheehan’s syndrome preceded by post partum hemorrhage. During investigations, they were found to have Pancytopenia with hypocellular marrow. Treatment with thyroxine and glucocorticoids resulted in complete recovery after attaining euthyroid and eucortisolemic state. Review of literature revealed the rarity of the disorder, with only four cases reported so far. Multiple anterior pituitary hormone deficiencies in Sheehan’s syndrome are responsible for Pancytopenia; replacement of thyroid and cortisol hormones results in complete recovery.

  • sheehan s syndrome with Pancytopenia complete recovery after hormone replacement case series with review
    Annals of Hematology, 2010
    Co-Authors: Bashir Ahmad Laway, Javid Rasool Bhat, Mohd Iqbal Lone, Shahnaz Ahmad Mir, Raja Sultan Zaman Khan, Abdul Hamid Zargar
    Abstract:

    Reports of Pancytopenia in patients with Sheehan’s syndrome are rare, because the disorder is not commonly seen in western countries. A case series of Pancytopenia in three patients of Sheehan’s syndrome is presented. Three women aged 22, 30, and 34 years developed Sheehan’s syndrome preceded by post partum hemorrhage. During investigations, they were found to have Pancytopenia with hypocellular marrow. Treatment with thyroxine and glucocorticoids resulted in complete recovery after attaining euthyroid and eucortisolemic state. Review of literature revealed the rarity of the disorder, with only four cases reported so far. Multiple anterior pituitary hormone deficiencies in Sheehan’s syndrome are responsible for Pancytopenia; replacement of thyroid and cortisol hormones results in complete recovery.

Javid Rasool Bhat - One of the best experts on this subject based on the ideXlab platform.

  • Hematological response of Pancytopenia to glucocorticoids in patients with Sheehan’s syndrome
    Pituitary, 2012
    Co-Authors: Bashir Ahmad Laway, Javid Rasool Bhat, Mohd Iqbal Lone, Jeelani Samoon, Abdul Hamid Zargar
    Abstract:

    Sheehan’s syndrome presents with panhypopituitarism after childbirth, usually preceded by post partum hemorrhage. Hematological abnormalities like Pancytopenia with hypocellular marrow in these patients are reported rarely. Though multiple hormone deficiencies may contribute to Pancytopenia in Sheehan’s syndrome, complete recovery is observed after achieving eucortisolemic and euthyroid state. The predominant role of thyroxine or glucocorticoids in reversing Pancytopenia in these patients has not been studied. We present the clinical, hormonal, hematological course and response to glucocorticoids in a patient of Sheehan’s syndrome presenting with Pancytopenia. Complete recovery of Pancytopenia was observed after achieving eucortisolemic state thus concluding that gulcocorticoid replacement is sufficient to reverse Pancytopenia in these patients.

  • Sheehan’s syndrome with Pancytopenia—complete recovery after hormone replacement (case series with review)
    Annals of Hematology, 2010
    Co-Authors: Bashir Ahmad Laway, Javid Rasool Bhat, Mohd Iqbal Lone, Shahnaz Ahmad Mir, Raja Sultan Zaman Khan, Abdul Hamid Zargar
    Abstract:

    Reports of Pancytopenia in patients with Sheehan’s syndrome are rare, because the disorder is not commonly seen in western countries. A case series of Pancytopenia in three patients of Sheehan’s syndrome is presented. Three women aged 22, 30, and 34 years developed Sheehan’s syndrome preceded by post partum hemorrhage. During investigations, they were found to have Pancytopenia with hypocellular marrow. Treatment with thyroxine and glucocorticoids resulted in complete recovery after attaining euthyroid and eucortisolemic state. Review of literature revealed the rarity of the disorder, with only four cases reported so far. Multiple anterior pituitary hormone deficiencies in Sheehan’s syndrome are responsible for Pancytopenia; replacement of thyroid and cortisol hormones results in complete recovery.

  • sheehan s syndrome with Pancytopenia complete recovery after hormone replacement case series with review
    Annals of Hematology, 2010
    Co-Authors: Bashir Ahmad Laway, Javid Rasool Bhat, Mohd Iqbal Lone, Shahnaz Ahmad Mir, Raja Sultan Zaman Khan, Abdul Hamid Zargar
    Abstract:

    Reports of Pancytopenia in patients with Sheehan’s syndrome are rare, because the disorder is not commonly seen in western countries. A case series of Pancytopenia in three patients of Sheehan’s syndrome is presented. Three women aged 22, 30, and 34 years developed Sheehan’s syndrome preceded by post partum hemorrhage. During investigations, they were found to have Pancytopenia with hypocellular marrow. Treatment with thyroxine and glucocorticoids resulted in complete recovery after attaining euthyroid and eucortisolemic state. Review of literature revealed the rarity of the disorder, with only four cases reported so far. Multiple anterior pituitary hormone deficiencies in Sheehan’s syndrome are responsible for Pancytopenia; replacement of thyroid and cortisol hormones results in complete recovery.

Mohd Iqbal Lone - One of the best experts on this subject based on the ideXlab platform.

  • Hematological response of Pancytopenia to glucocorticoids in patients with Sheehan’s syndrome
    Pituitary, 2012
    Co-Authors: Bashir Ahmad Laway, Javid Rasool Bhat, Mohd Iqbal Lone, Jeelani Samoon, Abdul Hamid Zargar
    Abstract:

    Sheehan’s syndrome presents with panhypopituitarism after childbirth, usually preceded by post partum hemorrhage. Hematological abnormalities like Pancytopenia with hypocellular marrow in these patients are reported rarely. Though multiple hormone deficiencies may contribute to Pancytopenia in Sheehan’s syndrome, complete recovery is observed after achieving eucortisolemic and euthyroid state. The predominant role of thyroxine or glucocorticoids in reversing Pancytopenia in these patients has not been studied. We present the clinical, hormonal, hematological course and response to glucocorticoids in a patient of Sheehan’s syndrome presenting with Pancytopenia. Complete recovery of Pancytopenia was observed after achieving eucortisolemic state thus concluding that gulcocorticoid replacement is sufficient to reverse Pancytopenia in these patients.

  • Sheehan’s syndrome with Pancytopenia—complete recovery after hormone replacement (case series with review)
    Annals of Hematology, 2010
    Co-Authors: Bashir Ahmad Laway, Javid Rasool Bhat, Mohd Iqbal Lone, Shahnaz Ahmad Mir, Raja Sultan Zaman Khan, Abdul Hamid Zargar
    Abstract:

    Reports of Pancytopenia in patients with Sheehan’s syndrome are rare, because the disorder is not commonly seen in western countries. A case series of Pancytopenia in three patients of Sheehan’s syndrome is presented. Three women aged 22, 30, and 34 years developed Sheehan’s syndrome preceded by post partum hemorrhage. During investigations, they were found to have Pancytopenia with hypocellular marrow. Treatment with thyroxine and glucocorticoids resulted in complete recovery after attaining euthyroid and eucortisolemic state. Review of literature revealed the rarity of the disorder, with only four cases reported so far. Multiple anterior pituitary hormone deficiencies in Sheehan’s syndrome are responsible for Pancytopenia; replacement of thyroid and cortisol hormones results in complete recovery.

  • sheehan s syndrome with Pancytopenia complete recovery after hormone replacement case series with review
    Annals of Hematology, 2010
    Co-Authors: Bashir Ahmad Laway, Javid Rasool Bhat, Mohd Iqbal Lone, Shahnaz Ahmad Mir, Raja Sultan Zaman Khan, Abdul Hamid Zargar
    Abstract:

    Reports of Pancytopenia in patients with Sheehan’s syndrome are rare, because the disorder is not commonly seen in western countries. A case series of Pancytopenia in three patients of Sheehan’s syndrome is presented. Three women aged 22, 30, and 34 years developed Sheehan’s syndrome preceded by post partum hemorrhage. During investigations, they were found to have Pancytopenia with hypocellular marrow. Treatment with thyroxine and glucocorticoids resulted in complete recovery after attaining euthyroid and eucortisolemic state. Review of literature revealed the rarity of the disorder, with only four cases reported so far. Multiple anterior pituitary hormone deficiencies in Sheehan’s syndrome are responsible for Pancytopenia; replacement of thyroid and cortisol hormones results in complete recovery.

Raja Sultan Zaman Khan - One of the best experts on this subject based on the ideXlab platform.

  • Sheehan’s syndrome with Pancytopenia—complete recovery after hormone replacement (case series with review)
    Annals of Hematology, 2010
    Co-Authors: Bashir Ahmad Laway, Javid Rasool Bhat, Mohd Iqbal Lone, Shahnaz Ahmad Mir, Raja Sultan Zaman Khan, Abdul Hamid Zargar
    Abstract:

    Reports of Pancytopenia in patients with Sheehan’s syndrome are rare, because the disorder is not commonly seen in western countries. A case series of Pancytopenia in three patients of Sheehan’s syndrome is presented. Three women aged 22, 30, and 34 years developed Sheehan’s syndrome preceded by post partum hemorrhage. During investigations, they were found to have Pancytopenia with hypocellular marrow. Treatment with thyroxine and glucocorticoids resulted in complete recovery after attaining euthyroid and eucortisolemic state. Review of literature revealed the rarity of the disorder, with only four cases reported so far. Multiple anterior pituitary hormone deficiencies in Sheehan’s syndrome are responsible for Pancytopenia; replacement of thyroid and cortisol hormones results in complete recovery.

  • sheehan s syndrome with Pancytopenia complete recovery after hormone replacement case series with review
    Annals of Hematology, 2010
    Co-Authors: Bashir Ahmad Laway, Javid Rasool Bhat, Mohd Iqbal Lone, Shahnaz Ahmad Mir, Raja Sultan Zaman Khan, Abdul Hamid Zargar
    Abstract:

    Reports of Pancytopenia in patients with Sheehan’s syndrome are rare, because the disorder is not commonly seen in western countries. A case series of Pancytopenia in three patients of Sheehan’s syndrome is presented. Three women aged 22, 30, and 34 years developed Sheehan’s syndrome preceded by post partum hemorrhage. During investigations, they were found to have Pancytopenia with hypocellular marrow. Treatment with thyroxine and glucocorticoids resulted in complete recovery after attaining euthyroid and eucortisolemic state. Review of literature revealed the rarity of the disorder, with only four cases reported so far. Multiple anterior pituitary hormone deficiencies in Sheehan’s syndrome are responsible for Pancytopenia; replacement of thyroid and cortisol hormones results in complete recovery.