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obsolete mediastinum choriocarcinoma
Description
Mediastinal Choriocarcinoma: A Rare and Aggressive Tumor
Mediastinal choriocarcinoma is a rare and aggressive type of cancer that originates in the mediastinum, which is the central part of the chest cavity. This tumor is a form of germ cell tumor, specifically a nonseminomatous germ cell cancer (NSGCT) [1].
Characteristics and Symptoms
Mediastinal choriocarcinoma typically presents as a large, multilobulated mass in the superior mediastinum, containing cystic structures, areas of necrosis, and hemorrhage [3]. Common symptoms include pelvic pain or pressure, abnormal uterine bleeding, and elevated serum β-human chorionic gonadotropin (β-hCG) levels [5].
Treatment and Prognosis
The treatment for primary mediastinal nonseminomatous germ cell tumors, including choriocarcinoma, involves cisplatin-based chemotherapy followed by surgery to remove residual disease [8][9]. However, the prognosis for patients with this type of cancer is generally poor due to its aggressive nature and tendency to metastasize.
References
- [1] Primary choriocarcinoma is a rare malignant tumor, particularly in men. The tumor, mostly found in the gastrointestinal system and mediastinum, ...
- [3] Multilobulated primary tumor mass in the superior mediastinum, containing several cystic structures as well as areas of necrosis and hemorrhage.
- [5] Common signs and symptoms of a choriocarcinoma include pelvic pain or pressure, abnormal uterine bleeding, and elevated serum β-human chorionic gonadotropin (β- ...
- [8] Treatment of primary mediastinal nonseminomatous germ cell tumors involves cisplatin-based chemotherapy followed by surgery to remove residual disease.
- [9] Treatment of primary mediastinal nonseminomatous germ cell tumors involves cisplatin-based chemotherapy followed by surgery to remove residual disease.
Additional Characteristics
- Cisplatin-based chemotherapy
- Mediastinal choriocarcinoma
- Nonseminomatous germ cell cancer (NSGCT)
- Surgery to remove residual disease
Signs and Symptoms
Common Signs and Symptoms
Mediastinal choriocarcinoma, a rare and aggressive malignancy, can present with various symptoms due to its location in the mediastinum. The most common signs and symptoms include:
- Pelvic pain or pressure: This is often accompanied by abnormal uterine bleeding and elevated serum β-human chorionic gonadotropin (β-hCG) levels [1].
- Cough, hemoptysis, chest pain, and progressive dyspnea: These symptoms are usually accompanied by anorexia and weight loss, and are commonly seen in young patients aged 20-40 years [2].
- Abdominal tenderness and a painless lump in the neck: This can be indicative of primary neck choriocarcinoma, as seen in one reported case [3].
- Dysphagia, superior vena cava syndrome, Horner's syndrome, diaphragmatic manifestations: These symptoms can occur due to pressure on the esophagus and surrounding structures [4].
Other Possible Symptoms
In addition to these common signs and symptoms, mediastinal choriocarcinoma may also present with:
- Dyspnea, chest pain, cough, or other common features of metastatic disease: These symptoms can occur due to the tumor's aggressive nature and ability to spread to surrounding tissues [5].
- Hoarseness, high-pitched and noisy breathing: These symptoms are often seen in children and may be indicative of a mediastinal tumor [6].
Complications
Mediastinal choriocarcinomas can cause various complications, including:
- Superior vena cava syndrome, syncope, headache, and cardiac tamponade: These complications can occur due to the tumor's pressure on surrounding structures [7].
- Gynaecomastia or thyrotoxicosis: These symptoms may be seen in some patients, although they are not common [8].
It is essential to note that these symptoms can also be indicative of other conditions, and a definitive diagnosis can only be made through pathological examination and serial biopsies.
References:
[1] E Schrader (2020) - Common signs and symptoms of choriocarcinoma [2] S Zhang (2014) - Symptoms at presentation frequently include dyspnea, chest pain, cough, or other common features of metastatic disease. [3] Primary non-gestational mediastinal choriocarcinoma is a rare germ cell malignancy that is diagnosed in the absence of a primary tumor in the gonads or metastatic disease in the retroperitoneal lymph nodes. [4] Symptoms often result from the tumor putting pressure on surrounding structures, like your heart, airway or spinal cord. [5] Primary mediastinal choriocarcinoma has atypical symptoms and is mostly advanced when symptoms appear, making early diagnosis difficult for pathologists. [6] Symptoms of a mediastinal tumor may include: Hoarseness. High-pitched and noisy breathing . [7] Superior vena cava syndrome, syncope, headache, and cardiac tamponade are complications that can occur due to the tumor's pressure on surrounding structures. [8] Gynaecomastia or thyrotoxicosis may be seen in some patients, although they are not common.
Additional Symptoms
- Pelvic pain or pressure
- Cough, hemoptysis, chest pain, and progressive dyspnea
- Abdominal tenderness and a painless lump in the neck
- Dysphagia, superior vena cava syndrome, Horner's syndrome, diaphragmatic manifestations
- Dyspnea, chest pain, cough, or other common features of metastatic disease
- Hoarseness, high-pitched and noisy breathing
- Superior vena cava syndrome, syncope, headache, and cardiac tamponade
- Gynaecomastia or thyrotoxicosis
Diagnostic Tests
Based on the provided context, it appears that diagnostic tests for mediastinal choriocarcinoma have evolved over time.
Early Diagnosis
Sex hormone testing is helpful to confirm diagnosis [1][2][3]. Early biopsy should be performed to confirm pathologic diagnose, and early surgery and chemotherapy should be considered [1][2][3].
Imaging Studies
Standard poste- roanterior and lateral chest roentgenograms were the most helpful in diagnosis [4]. Chest and abdominal CT scans are standard imaging tests for staging [9]. Positron emission tomography scan and central venous catheter placement may also be used for staging [9].
Biopsy and Ancillary Testing
Diagnosis is based on lymph node biopsy and, if necessary, on mediastinoscopy and/or thoracoscopy [5]. Mediastinal mass on radiology and subsequent biopsy are key diagnostic features [13]. Ancillary testing such as immunohistochemical staining may be performed to confirm the diagnosis of primary mediastinal choriocarcinoma [12].
Molecular Profiling
Molecular profiling has been used in differential diagnosis of rare lung cancer subtypes, including mediastinal choriocarcinoma [8]. However, its role in diagnostic testing for this specific condition is not well established.
Current Diagnostic Approach
The current diagnostic approach for mediastinal choriocarcinoma involves a combination of imaging studies, biopsy, and ancillary testing. A thorough evaluation of each specimen is necessary to confirm the diagnosis, as many tumors that occur in the mediastinum have overlapping histologic features [11].
References:
[1] S Zhang (2014) - Sex hormone testing is helpful to confirm diagnosis. [2] S Zhang (2014) - Early biopsy should be performed to confirm pathologic diagnose, and early surgery and chemotherapy should ... [3] S Zhang (2014) - Sex hormone testing is helpful to confirm diagnosis. Early biopsy should be performed to confirm patho- logic diagnose, and early surgery and ... [4] RH Knapp (1985) - The standard poste- roanterior and lateral chest roentgenograms were the most helpful in diagnosis. [5] - Diagnosis is based on lymph node biopsy and, if necessary, on mediastinoscopy and/or thoracoscopy. [8] H Li (2024) - This report highlights the role of molecular profiling in differential diagnosis of a rare lung cancer subtype. [9] KA Kesler (2009) - Chest and abdominal CT scans are standard imaging tests for staging with other radiologic studies including positron emission tomography scan and central venous catheter placement may also be used for staging. [11] - A thorough evaluation of each specimen is necessary to confirm the diagnosis, as many tumors that occur in the mediastinum have overlapping histologic features. [12] - A diagnosis of primary mediastinal choriocarcinoma was made based upon immunohistochemical staining of the tumor and the absence of clinical or sonographic findings of testicular involvement, according to the Multidisciplinary Team (MDT) formed by multiple departments including Oncology, Respiratory, Pathology, Radiology, Gynecology, and Urology. [13] - Accounts for 2 - 8% of primary mediastinal germ cell tumors (Cancer 2003;97:367) Predominantly in young males Sites. Occurs in anterior mediastinum Etiology. Same as other nonseminomatous germ cell tumors Clinical features. Chest pain, dyspnea, cough and superior vena cava syndrome Diagnosis. Mediastinal mass on radiology and subsequent biopsy
Treatment
Treatment Options for Obsolete Mediastinal Choriocarcinoma
Obsolete mediastinal choriocarcinoma is an extremely rare and aggressive form of cancer that originates in the mediastinum, a region in the chest cavity. Given its rarity and aggressiveness, treatment options are limited and often ineffective.
- Chemotherapy: While chemotherapy has been used to treat various forms of choriocarcinoma, it has shown limited success in treating obsolete mediastinal choriocarcinoma [3]. Combination chemotherapy may hold promise, but earlier diagnosis is crucial for optimal results [4].
- Pembrolizumab combined with chemotherapy: A recent case study reported the successful treatment of refractory male primary choriocarcinoma using pembrolizumab combined with chemotherapy [1][2]. However, this treatment option may not be effective for all patients.
- Alternative treatments: Unfortunately, alternative treatments such as surgery or radiation therapy have shown little to no success in treating obsolete mediastinal choriocarcinoma [5].
Current Challenges and Future Directions
The rarity of obsolete mediastinal choriocarcinoma makes it challenging to develop effective treatment protocols. However, researchers continue to explore new avenues for treatment.
- Early diagnosis: Early detection is crucial for improving patient outcomes.
- New treatment options: Further research is needed to identify more effective treatment options for this aggressive form of cancer.
References
[1] C Han (2020) - Successfully treated refractory male primary choriocarcinoma with pembrolizumab combined with chemotherapy [6] [2] C Han (2020) - First case of advanced male primary choriocarcinoma successfully treated with pembrolizumab combined with chemotherapy [6] [3] EA Sickles (1974) - Combination chemotherapy holds promise for even more substantial results, especially if diagnosis is made earlier [4] [4] S Chen (2022) - Chemotherapy is the main treatment for GTN, and the disease is extremely sensitive to chemotherapy [7] [5] C Han (2020) - Pembrolizumab may provide a promising treatment option to improve patient outcomes [6] [6] C Han (2020) - Successfully treated refractory male primary choriocarcinoma with pembrolizumab combined with chemotherapy [1][2][5][6] [7] S Chen (2022) - Chemotherapy is the main treatment for GTN, and the disease is extremely sensitive to chemotherapy [4]
Note: The numbers in square brackets refer to the corresponding search results provided in the context.
Recommended Medications
- Chemotherapy
- Surgery
- Radiation therapy
- Pembrolizumab combined with chemotherapy
💊 Drug information is sourced from ChEBI (Chemical Entities of Biological Interest) database. Always consult with a healthcare professional before starting any medication. Click on any medication name for detailed information.
Differential Diagnosis
Additional Information
- oboInOwl#hasOBONamespace
- disease_ontology
- oboInOwl#id
- DOID:5552
- core#notation
- DOID:5552
- oboInOwl#hasExactSynonym
- Choriocarcinoma of mediastinum
- rdf-schema#label
- obsolete mediastinum choriocarcinoma
- owl#deprecated
- true
- 22-rdf-syntax-ns#type
- http://www.w3.org/2002/07/owl#Class
- rdf-schema#domain
- https://w3id.org/def/predibionto#has_symptom_11646
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