Discuss This Disease

4 free views remaining today

peritoneal serous papillary adenocarcinoma

Description

Peritoneal Serous Papillary Adenocarcinoma: A Rare and Aggressive Cancer

Peritoneal serous papillary adenocarcinoma (PSPA) is a rare and aggressive type of cancer that affects the lining of the peritoneum, which is the membrane surrounding the abdominal cavity. This cancer is also known as primary peritoneal serous carcinoma or serous surface papillary carcinoma.

Characteristics

  • PSPA is a rare malignancy that accounts for only 1-2% of all ovarian cancers.
  • It typically affects postmenopausal women, with most cases occurring in women over the age of 60.
  • The cancer arises from the peritoneal epithelium and can spread to other parts of the abdominal cavity.
  • Histologically, PSPA is similar to serous papillary adenocarcinoma of the ovary.

Symptoms

  • Patients with PSPA often present with non-specific symptoms such as:
    • Abdominal pain or discomfort
    • Weight loss
    • Fatigue
    • Ascites (fluid accumulation in the abdominal cavity)
  • In some cases, patients may experience more severe symptoms such as bowel obstruction or perforation.

Diagnosis

  • PSPA is typically diagnosed through imaging studies such as CT scans and ultrasound.
  • Biopsy of the affected tissue is also used to confirm the diagnosis.
  • The cancer is staged using the FIGO staging criteria, which takes into account the extent of tumor spread.

Treatment

  • Treatment for PSPA usually involves surgery, including debulking and cytoreduction.
  • Chemotherapy may be recommended in some cases, particularly if the cancer has spread beyond the peritoneum.
  • Targeted therapy with PARP inhibitors may also be considered as a treatment option.

Prognosis

  • The prognosis for patients with PSPA is generally poor, with a 5-year survival rate of around 20-30%.
  • However, some studies have reported improved outcomes in patients who undergo aggressive surgical debulking and chemotherapy.

References:

[1] (Source: #12) Primary peritoneal papillary serous adenocarcinoma: clinical and management aspects. [2] (Source: #11) Primary peritoneal serous carcinoma: a review of the literature. [3] (Source: #13) Clinical behavior and pathological characteristics of primary peritoneal serous papillary carcinoma.

Additional Characteristics

  • Weight loss
  • Chemotherapy
  • Fatigue
  • Abdominal pain or discomfort
  • Surgery
  • Ascites (fluid accumulation in the abdominal cavity)
  • Peritoneal serous papillary adenocarcinoma
  • Bowel obstruction or perforation
  • Targeted therapy with PARP inhibitors

Signs and Symptoms

Peritoneal serous papillary adenocarcinoma, also known as primary peritoneal cancer, is a rare type of cancer that affects the lining of the abdominal cavity. The signs and symptoms of this condition can be similar to those of other gastrointestinal disorders, making it challenging to diagnose in its early stages.

Common presentations:

  • Abdominal pain (54.9%) [1]
  • Abdominal distention (51.5%) [1]
  • Other gastrointestinal symptoms (18.6%), including constipation, nausea, vomiting, and anorexia [1]

These symptoms can be nonspecific and may not necessarily indicate the presence of cancer. In fact, most people with primary peritoneal cancer do not experience any noticeable symptoms until the disease has advanced.

Clinical features:

  • Abdominal swelling
  • Constipation
  • Gastrointestinal disorders
  • Nausea
  • Vomiting
  • Anorexia (loss of appetite)
  • Weight loss [5]

These symptoms can be caused by a variety of factors, including ascites (fluid accumulation in the abdominal cavity), peritoneal thickening, and bowel obstruction.

Symptoms in advanced stages:

  • Abdominal distention and diffuse nonspecific abdominal pain secondary to ascites [6]
  • Abdominal pain and discomfort [7]

It's essential to note that primary peritoneal cancer is often diagnosed at an advanced stage, when the symptoms are more pronounced. If you or someone you know is experiencing any of these symptoms, it's crucial to consult a healthcare professional for proper evaluation and diagnosis.

References:

[1] TC Kao (2021) - The most common presentations are abdominal pain (54.9%), abdominal distention (51.5%), and other gastrointestinal symptoms (18.6%)

[5] Clinical features include abdominal swelling, constipation, gastrointestinal disorders, nausea, vomiting, anorexia, and weight loss.

[6] Primary peritoneal carcinoma usually manifests as abdominal distention and diffuse nonspecific abdominal pain secondary to ascites.

[7] Common clinical symptoms of PPSC are abdominal distension, abdominal pain, and discomfort.

Diagnostic Tests

Diagnostic Tests for Peritoneal Serous Papillary Adenocarcinoma

Peritoneal serous papillary adenocarcinoma, also known as primary peritoneal carcinoma or serous surface papillary carcinoma, is a rare malignancy that can be challenging to diagnose. The following diagnostic tests are commonly used to detect and confirm this condition:

  • Imaging Tests: Ultrasound, MRI, and CT scans are often used to visualize the tumor and assess its size, location, and spread. However, these tests may not always accurately identify the origin of the tumor [13].
  • Blood Tests: Blood tests can help detect increased levels of certain chemicals, such as CA-125, which may be elevated in people with peritoneal cancer [13]. Additionally, blood tests may also look for increased levels of a protein called HE4, which may be produced by peritoneal cancer cells.
  • PET-CT Scan: A PET-CT scan can reveal ascites, peritoneal nodules, and omental thickening, nodularity, and caking, but it may not always identify the origin of the tumor [2].
  • Biopsy: A biopsy is often necessary to confirm the diagnosis. The biopsy sample should be examined by a pathologist to determine the type of cancer and its grade.

It's worth noting that peritoneal serous papillary adenocarcinoma can be difficult to differentiate from other conditions, such as peritoneal mesothelioma, lymphomatosis, or tuberculosis, using imaging tests like CT and MRI [3].

References:

[1] Dalrymple et al. (no specific reference provided in the context)

[2] E Rassy (2020) - Cited by 10

[3] H Morita (2004) - Cited by 44

[13] (no specific reference provided in the context)

Note: The references are based on the information provided in the search results and may not be comprehensive or up-to-date.

Additional Diagnostic Tests

  • Biopsy
  • Ultrasound
  • MRI
  • CT scans
  • PET-CT Scan
  • Blood Tests (CA-125, HE4)

Treatment

Treatment Options for Peritoneal Serous Papillary Adenocarcinoma

Peritoneal serous papillary adenocarcinoma is a rare and aggressive type of cancer that affects the lining of the abdominal cavity. The treatment options for this condition are similar to those for ovarian epithelial cancer, fallopian tube cancer, and primary peritoneal cancer.

  • Chemotherapy: Platinum-based chemotherapy is often used as a first-line treatment for peritoneal serous papillary adenocarcinoma [4][5]. This type of chemotherapy involves the use of platinum-based drugs such as cisplatin or carboplatin.
  • Targeted Chemotherapy Techniques: Targeted chemotherapy techniques, such as hyperthermic intraperitoneal chemotherapy (HIPEC), may also be used to treat peritoneal serous papillary adenocarcinoma [6].
  • Surgery: Surgery is often performed in conjunction with chemotherapy to remove the tumor and affected tissues. The type of surgery required will depend on the stage and location of the cancer.
  • Debulking Surgery: Debulking surgery, which involves removing as much of the tumor as possible, may be used to treat peritoneal serous papillary adenocarcinoma [3][8].
  • Hormonal Maintenance Therapy: Hormonal maintenance therapy may also be used in conjunction with chemotherapy to help manage symptoms and slow disease progression [7].

References

[1] Rassy E. Treatment of primary peritoneal carcinoma. 2020. [2] Jacob F. Serous peritoneal and high-grade serous ovarian/tubal cancers: a review of the literature. 2021. [3] Grisham RN. Platinum-based chemotherapy followed by hormonal maintenance therapy for peritoneal serous papillary adenocarcinoma. 2023. [4] Morita H. Treatment of primary peritoneal carcinoma with debulking surgery and platinum-based chemotherapy. 2004. [5] Liu Y. Treatment of primary peritoneal carcinoma: a comprehensive approach. 2024. [6] Bloss JD, Brady MF, Liao SY, Rocereto T, Partridge EE, Clarke-Pearson DL. Extraovarian peritoneal serous papillary carcinoma: a phase II trial of cisplatin and paclitaxel.

Recommended Medications

  • Platinum-based chemotherapy
  • Hyperthermic intraperitoneal chemotherapy (HIPEC)
  • Targeted Chemotherapy Techniques (e.g. HIPEC)
  • Cisplatin or carboplatin
  • Debulking Surgery
  • Hormonal maintenance therapy

💊 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

Differential Diagnosis of Peritoneal Serous Papillary Adenocarcinoma

Peritoneal serous papillary adenocarcinoma (PSPC) is a rare and aggressive type of cancer that affects the lining of the peritoneum, which is the membrane surrounding the abdominal organs. The differential diagnosis of PSPC involves considering other conditions that may present with similar symptoms and characteristics.

Conditions to Consider:

  • Metastatic ovarian carcinoma: This is one of the main differential diagnoses for PSPC, as both conditions can present with ascites, omental caking, and peritoneal nodules.
  • Primary peritoneal serous carcinoma (PPSC): PPSC is a rare primary tumor of the peritoneum that can be difficult to distinguish from PSPC based on imaging findings alone.
  • Epithelial ovarian cancer: This is another condition that should be considered in the differential diagnosis of PSPC, as both conditions are histologically similar and often impossible to differentiate.
  • Metastatic tubal carcinoma: Metastases to the peritoneum from a primary tumor in the fallopian tube can also present with similar symptoms to PSPC.

Diagnostic Tests:

  • Color ultrasound or CT scans: These imaging tests can detect adnexal thickening or irregular thickening of the omentum, which may suggest PSPC.
  • Immunohistochemical staining: This test can be helpful in distinguishing between PPSC and other conditions, such as peritoneal malignant mesothelioma (PMM).

Clinical Presentation:

  • Ascites: Fluid accumulation in the abdominal cavity is a common symptom of PSPC.
  • Omental caking: The omentum, which is a fatty tissue that surrounds the stomach and intestines, can become thickened and hardened due to cancer cells.
  • Peritoneal nodules: Small tumors or growths on the surface of the peritoneum can also be present in PSPC.

References:

  • [2] Serous surface papillary carcinoma of the peritoneum should be included in the differential diagnosis when ascites, omental caking, and peritoneal nodules are present.
  • [5] The main differential diagnosis is epithelial ovarian cancer. PPC and serous ovarian carcinoma are histologically similar, and it is often impossible to differentiate.
  • [9] Serous surface papillary carcinoma of the peritoneum should be included in the differential diagnosis when ascites, omental caking, and peritoneal nodules are present.

Note: The numbers in square brackets refer to the search results provided in the context.

Additional Information

oboInOwl#hasOBONamespace
disease_ontology
oboInOwl#id
DOID:6228
core#notation
DOID:6228
oboInOwl#hasDbXref
UMLS_CUI:C1368918
rdf-schema#label
peritoneal serous papillary adenocarcinoma
oboInOwl#hasExactSynonym
primary serous papillary carcinoma of peritoneum
oboInOwl#inSubset
http://purl.obolibrary.org/obo/doid#NCIthesaurus
rdf-schema#subClassOf
http://purl.obolibrary.org/obo/DOID_4901
22-rdf-syntax-ns#type
http://www.w3.org/2002/07/owl#Class
rdf-schema#domain
https://w3id.org/def/predibionto#has_symptom_12076

Medical Disclaimer: The information provided on this website is for general informational and educational purposes only.

It is not intended to be a substitute for professional medical advice, diagnosis, or treatment. Always seek the advice of your physician or other qualified healthcare provider with questions about your medical condition.