Key Documents
Uma N. Sundram, MD, PhD
Academic Appointments
- Assistant Professor - Med Center Line, Pathology
- Assistant Professor - Med Center Line, Dermatology
Contact Information
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Clinical Offices
Department of Pathology 300 Pasteur Dr H2110 MC 5324 Stanford, CA 94305 Tel Work (650) 723-7211 Fax (650) 725-7409Practices at Stanford Hospital and Clinics and Lucile Packard Children's Hospital
- Academic Offices
Administrative Contact Darlene Washington Administrative Assistant Email Tel Work 650-725-0405Not for medical emergencies or patient use
Professional Snapshot
Clinical Focus
- Pathology
- Anatomic/Clinical Pathology
Professional Education
| Board Certification: | Dermatopathology, American Board of Pathology (2004) |
| Board Certification: | Anatomic Pathology, American Board of Pathology (2003) |
| Fellowship: | Stanford University Medical Center, CA (2003) |
| Residency: | Stanford University Medical Center, CA (2002) |
| Internship: | Stanford University Medical Center, CA (2000) |
Web Site Links
Scientific Focus
Research Interests
My research program is primarily centered on the exploration of mechanisms driving hematopoietic disorders in the skin. Compared to hematopoietic disorders (lymphomas, leukemias, and mast cell disease) that involve other organs in the body, such as the lymph node, bone marrow, and spleen, the counterparts of these diseases in the skin have a different clinical presentation, course, and outcome. For example, patients with the most common lymphoma that starts in the skin, mycosis fungoides, can have a long and fruitful life, if the disease is limited to the skin and does not involve other organs in the body. For this reason, clinicians usually treat these patients with more conservative therapies (such as topical steroids) to control the disease, rather than with systemic chemotherapy, as in the case of their systemic counterparts. The most common type of mast cell disease of the skin, urticaria pigmentosa, occurs frequently in children, and can regress before puberty. On the other hand, adult patients with mast cell disease that involve organs other than skin can have a more aggressive clinical course, with a subset of these patients dying from their disease. Although the characteristics of the genes and proteins that cause these diseases are currently being studied, a key discovery would lie in our ability to distinguish patients who are going to do well (because their disease will be limited to the skin) from patients who may not do as well. The importance of this distinction would be in the therapeutic approach: patients with more aggressive disease would get more aggressive therapy. Unfortunately, cutaneous lymphomas are notoriously difficult to diagnose accurately, as they can look very much like reactive processes under the microscope. Similarly, although it is relatively straightforward to render the diagnosis of mast cell disease in the skin, distinguishing mast cell disease that will spontaneously regress from those that will have a more aggressive clinical course...
Publications
- Low stage follicular lymphoma: biologic and clinical characterization according to nodal or extranodal primary origin. Am J Surg Pathol. 2009; (4): 591-8
- A malignant cutaneous neuroendocrine tumor with features of Merkel cell carcinoma and differentiating neuroblastoma. Am J Dermatopathol. 2009; (2): 193-6
- Cutaneous peripheral T-cell lymphoma associated with a proliferation of B cells. Am J Clin Pathol. 2009; (6): 810-9
- Review: Dermatofibrosarcoma protuberans: histologic approach and updated treatment recommendations. Clin Adv Hematol Oncol. 2009; (6): 406-8
- Persistent scale in the diaper area. Pediatr Dermatol. 2008 Jul-Aug; (4): 477-8

