MBBS, MPhil (Oncology)
Cancer Specialist
🎯 Osteosarcoma management, Ewing sarcoma, Chondrosarcoma care, Chordoma management, Gastrointestinal stromal
View Profile →Oncologist (Oncology)
MBBS, BCS (Health), MD (Oncology)
Cancer Specialist
🎯 Expert in treating: Desmoplastic small, Alveolar soft, Epithelioid hemangioendothelioma, Clear cell, Inflammatory myofibroblastic
🎓 Assistant Professor, Oncology & Radiotherapy Department
🏛️ Khulna Medical College & Hospital, Khulna
Assistant Professor, Oncology & Radiotherapy Department — Khulna Medical College & Hospital, Khulna
Asst. Prof. Dr. Shabnam Sultana best Oncologist and Cancer Specialist in Khulna City delivers specialized diagnostic, clinical, and therapeutic care for exceptionally rare soft tissue and vascular malignancies, including desmoplastic small round cell tumors (DSRCT), alveolar soft part sarcomas (ASPS), and epithelioid hemangioendotheliomas (EHE). Looking for the best Cancer Specialist in Khulna, individuals consult her for precise clear cell sarcoma management, inflammatory myofibroblastic tumor (IMT) care, and comprehensive adult clinical oncological interventions. Her clinical practice spans aggressive, rare sarcomas, complex solid tumors, and advanced systemic chemoradiation. She integrates over 13 years of diagnostic wisdom with targeted medical and radiation therapies to optimize patient survival and manage life-threatening oncological conditions.
🏥 Top Choice Diagnostic Centre, Khulna · Diagnostic Center
📍 37, Shamsur Rahman Road, Shantidham Mor, Khulna
🕒 Visiting hours: 3:00pm to 5:00pm (Closed: Friday)
💳 Consultation fee: ৳800
Asst. Prof. Dr. Shabnam Sultana is an Assistant Professor in the Oncology & Radiotherapy Department at Khulna Medical College & Hospital, Khulna, with over 13 years of distinguished clinical, academic, and systemic cancer care experience. As an eminent Clinical Oncologist, she provides expert care for severe and exceedingly rare malignancies, with a highly specialized focus on soft tissue sarcomas and vascular tumors such as DSRCT, ASPS, EHE, clear cell sarcoma, and inflammatory myofibroblastic tumors. Patients seeking expert oncological evaluation receive evidence-based treatments tailored to halt disease progression, manage acute cancer-related crises, and achieve long-term remission. Her medical practice combines high-precision cancer diagnostics with individualized, systemic, and radiation-based patient care plans.
Dr. Shabnam Sultana completed her MBBS degree, establishing a robust clinical foundation in general medical sciences. Demonstrating a profound commitment to advanced cancer care, she entered the prestigious BCS (Health) cadre and pursued highly rigorous postgraduate specialization, earning her Doctor of Medicine (MD) in Oncology. This premier clinical qualification equips her with the dual expertise of a Clinical Oncologist—mastering both systemic medical oncology (chemotherapy and targeted therapy) and precision radiation oncology. Finding the best Oncologist in Khulna leads patients to rely on her 13+ years of academic leadership and specialized clinical expertise at Khulna Medical College & Hospital, a premier government medical institution.
Her primary clinical focus includes intensive multi-agent chemotherapy protocols for aggressive DSRCTs, targeted anti-angiogenic therapies for alveolar soft part sarcomas, specialized systemic management and surveillance for epithelioid hemangioendotheliomas, and ALK-inhibitor therapies for inflammatory myofibroblastic tumors. Her diagnostic framework incorporates advanced PET-CT scan analysis, deep molecular and immunohistochemistry (IHC) profiling, and comprehensive oncological risk stratification to formulate effective, long-term cancer survival strategies for extremely rare diagnoses.
| Profile Field | Details |
| Full Name | Asst. Prof. Dr. Shabnam Sultana |
| Primary Specialty | Clinical Oncology (Medical & Radiation) |
| Secondary Specialties | Rare Soft Tissue Sarcomas & Vascular Tumors |
| Designation | Assistant Professor, Oncology & Radiotherapy Department |
| Workplace | Khulna Medical College & Hospital, Khulna |
| Total Experience | 13+ Years |
| Location | Khulna, Bangladesh |
MBBS – Bachelor of Medicine and Bachelor of Surgery
BCS (Health) – Bangladesh Civil Service (Health Cadre)
MD (Oncology) – Doctor of Medicine in Oncology
Designation: Assistant Professor, Oncology & Radiotherapy Department
Workplace: Khulna Medical College & Hospital, Khulna
Desmoplastic small round cell tumor (DSRCT) requires highly aggressive multi-agent chemotherapy and radiation.
Alveolar soft part sarcoma (ASPS) demands targeted anti-angiogenic therapies and surgical planning.
Epithelioid hemangioendothelioma (EHE) requires specialized vascular tumor surveillance and systemic therapies.
Clear cell sarcoma (of soft tissue) needs molecular-targeted biological agents and localized radiation.
Inflammatory myofibroblastic tumor (IMT) demands targeted ALK-inhibitor therapy and surgical resection.
Breast cancer requires post-operative radiation and systemic hormonal/chemotherapy.
Lung cancer demands concurrent chemoradiation or targeted biological agents.
Colorectal cancer requires neoadjuvant or adjuvant chemotherapy and radiotherapy.
Head and neck cancers demand highly precise curative radiation therapy.
Cervical cancer demands external beam radiation combined with brachytherapy.
Ovarian cancer demands systemic platinum-based chemotherapy.
Gastric (Stomach) cancer needs systemic oncological evaluation and chemotherapy.
Brain metastasis demands whole-brain radiation to preserve neurological function.
Bone metastasis requires palliative radiation for rapid pain relief and fracture prevention.
Lymphomas (Hodgkin & Non-Hodgkin) require specialized systemic immunochemotherapy.
Rare Soft Tissue Sarcomas: Precision management for incredibly rare cancers of the connective tissues, muscles, and blood vessels, requiring advanced molecular testing to guide highly specific targeted therapies.
Clinical Oncology (Dual Expertise): Comprehensive delivery of both systemic intravenous chemotherapy and targeted external beam radiation therapy, preventing the need to transfer patients between different specialists.
General Solid Tumor Management: Expert, evidence-based management of common cancers (breast, lung, cervical, GI tract) utilizing 13 years of clinical experience in a major tertiary hospital.
For rare tumors like Clear Cell Sarcoma or EHE, looking at cells under a standard microscope is insufficient. Dr. Sultana utilizes advanced Immunohistochemistry (IHC) and molecular genetic testing (like checking for the EWSR1-WT1 gene fusion in DSRCT or ALK gene rearrangements in IMT). Identifying these exact genetic mutations dictates whether a tumor will respond to specific, modern targeted oral chemotherapy drugs.
Traditional chemotherapy often fails against rare sarcomas like ASPS. Instead, Dr. Sultana utilizes targeted therapies and anti-angiogenic drugs (which stop the tumor from growing new blood vessels). By cutting off the blood supply or blocking specific mutated proteins, she can halt the progression of cancers that were previously considered untreatable.
As a Clinical Oncologist, Dr. Sultana designs and oversees complex 3D-Conformal Radiation Therapy (3D-CRT) and intensity-modulated plans for both rare sarcomas and common solid tumors. She meticulously calculates the radiation dosage to shrink the tumor pre-surgery or destroy microscopic cancer cells post-surgery while maximally sparing surrounding healthy, vital organs.
An extremely rare, highly aggressive type of soft tissue sarcoma that primarily affects adolescent and young adult males. It typically presents as multiple tumors scattered throughout the abdomen and pelvis (the peritoneum). Because it grows rapidly and spreads early, treatment is gruelingly intense, requiring a combination of massive systemic chemotherapy, extensive abdominal surgery, and whole-abdomen radiation therapy.
A very rare, slow-growing but highly dangerous soft tissue sarcoma that typically arises in the deep muscles of the thigh or leg in young adults. Despite growing slowly, it has a high tendency to spread (metastasize) early to the lungs and brain through the bloodstream. It does not respond well to standard chemotherapy, requiring Dr. Sultana to use highly specialized targeted drugs (tyrosine kinase inhibitors).
An exceedingly rare vascular cancer that grows from the cells lining the inside of blood vessels. It can appear anywhere but most commonly affects the liver, lungs, and bones. Its behavior is highly unpredictable—in some patients, it remains dormant for years, while in others, it grows rapidly and aggressively. Management requires expert, highly individualized surveillance and targeted treatments.
Asst. Prof. Dr. Shabnam Sultana utilizes over 13 years of profound clinical wisdom to approach highly complex, life-threatening malignancies. Her philosophy emphasizes an exhaustive, molecular-level diagnostic approach to unearth rare soft tissue sarcomas, prioritizing the integration of modern targeted therapies over generalized treatments, and providing compassionate, systemic care for patients facing daunting and often misunderstood cancer diagnoses.
Emergency Callout: Immediate emergency medical evaluation is required if a chemotherapy patient develops a fever over 100.4°F (38°C) with chills (Febrile Neutropenia - a life-threatening lack of immune cells), a patient with abdominal tumors (like DSRCT) develops sudden severe abdominal pain and cannot pass gas or stool (bowel obstruction), or a sarcoma patient experiences sudden, severe breathlessness or coughing up blood (pulmonary metastasis/embolism).
Member, Bangladesh Medical and Dental Council (BMDC)
Assistant Professor, BCS (Health) Cadre
Member, Oncology Club, Bangladesh
Bring all prior biopsy reports, crucial immunohistochemistry (IHC) markers, molecular testing results, and recent PET-CT or MRI scans.
Maintain a complete list of current prescription medications and any previous chemotherapy discharge summaries.
Keep a detailed symptom diary noting new lumps, unexplained weight loss, deep muscle pain, or abdominal swelling.
Ensure a family member accompanies the patient to take detailed notes, as treatments for rare sarcomas involve highly complex, multi-drug regimens and side-effect management strategies.
Last Modified: October 27, 2026
Carcinomas are the most common cancers (like breast, lung, or colon cancer) and originate in the skin or tissues lining internal organs. Sarcomas are very rare cancers that originate in the body's connective tissues—such as muscles, fat, blood vessels, nerves, and bones. Because they are biologically distinct, sarcomas require specialized oncology protocols and distinct targeted therapies.
An MD (Doctor of Medicine) in Oncology is the highest clinical postgraduate degree focused entirely on the intricate pathology, diagnosis, and comprehensive treatment of cancer. Holding this degree allows Dr. Sultana to function as a "Clinical Oncologist," meaning she is fully trained and legally certified to prescribe and administer both systemic chemotherapy and targeted radiation therapy.
DSRCT is notoriously difficult to treat because it rarely forms a single, easily removable lump. Instead, it spreads like a web of hundreds of small tumors across the lining of the abdomen (the peritoneum). It requires a devastatingly aggressive combination of high-dose chemotherapy to shrink the tumors, massive surgery, and radiation to destroy the microscopic cells left behind.
IMT is a rare tumor that consists of inflammatory cells and spindle cells (myofibroblasts). It can occur anywhere in the body but is most common in the lungs and abdomen. While some are benign, others grow aggressively and can become malignant. Many IMTs are driven by a specific genetic mutation (the ALK gene), which Dr. Sultana can target with specific oral medications (ALK inhibitors) to shrink the tumor.
Unlike most soft tissue sarcomas that spread primarily through the lymphatic system (lymph nodes), ASPS uniquely invades the local blood vessels very early on. This allows the cancer cells to travel through the bloodstream, most frequently spreading (metastasizing) to the lungs and the brain, making early detection and brain MRI screenings critical.
Also known as "melanoma of soft parts," Clear Cell Sarcoma is a rare, aggressive tumor that typically arises in the deep tissues, tendons, and aponeuroses of the feet, ankles, and legs in young adults. It shares genetic similarities with malignant melanoma (skin cancer) but is a distinct disease requiring surgical resection and localized radiation.
Because EHE grows from the lining of blood vessels, its behavior varies wildly. If the tumor is completely asymptomatic and growing very slowly, Dr. Sultana may recommend "active surveillance" (watch and wait with frequent scans). If it becomes aggressive, she utilizes targeted anti-angiogenic drugs or coordinates with surgeons for liver or lung resections.
Not necessarily. Standard intravenous chemotherapy attacks all rapidly dividing cells, which predictably causes hair loss. Modern targeted therapies (often in pill form) are designed to seek out only specific mutated proteins on the cancer cells, leaving normal cells alone. While they have their own unique side effects, complete hair loss is much less common with targeted drugs.
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