Pediatrician, Dermatologist
10 years of experience
Video profile
Accepting new patients
Family Dermatology
929 S Tamiami Trl
Ste 204
Osprey, FL 34229
941-918-1900
Locations and availability (3)

Education ?

Medical School Score Rankings
Johns Hopkins University (2000)
Dermatology
  • Currently 4 of 4 apples
Top 25%
Residency
Boston Combined Residency Program (2003) *
Pediatrics
* This information was reported to Vitals by the doctor or doctor's office.

Awards & Distinctions ?

Awards  
Patients' Choice 5th Anniversary Award (2012 - 2013)
Patients' Choice Award (2008 - 2013)
Compassionate Doctor Recognition (2010 - 2013)
Associations
American Board of Dermatology

Affiliations ?

Dr. Gruman is affiliated with 3 hospitals.

Hospital Affilations

Score

Rankings

  • Manatee Memorial Hospital
    206 2nd St E, Bradenton, FL 34208
    • Currently 4 of 4 crosses
    Top 25%
  • Sarasota Memorial Hospital
    1700 S Tamiami Trl, Sarasota, FL 34239
    • Currently 4 of 4 crosses
    Top 25%
  • Doctors Hospital Of Sarasota *
    5731 Bee Ridge Rd, Sarasota, FL 34233
    • Currently 3 of 4 crosses
    Top 50%
  • Publications & Research

    Dr. Gruman has contributed to 1 publication.
    Title Kaposiform Hemangioendothelioma Without Kasabach-merritt Phenomenon.
    Date May 2006
    Journal Journal of the American Academy of Dermatology
    Excerpt

    Kasabach-Merritt phenomenon is a serious coagulopathy associated with kaposiform hemangioendothelioma (KHE), tufted angioma, and possibly other vascular neoplasms. KHE presenting in the absence of Kasabach-Merritt phenomenon is rare, although tufted angioma frequently occurs without thrombocytopenia. We retrospectively reviewed 10 cases of KHE without Kasabach-Merritt phenomenon. The tumors appeared as soft tissue masses with the overlying skin being either normal, erythematous, or violaceous. There were no radiologic or microscopic differences in noncoagulopathic KHE as compared with coagulopathic KHE. Evidence of platelet trapping and hemosiderin deposition was seen histologically, despite normal serum platelet levels. All KHE were less than 8 cm in diameter, suggesting that tumors that grow no larger than this size are less likely to trap platelets in sufficient quantity to cause thrombocytopenia. Our series confirms that KHE appears with a wide spectrum of behavior and response to treatment. The decision as to whether or not to treat a noncoagulopathic KHE should be based on the size and location of the tumor and the possible side effects of therapy.


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