scholarly journals Chronic ectopic pregnancy complicated by septicemic shock and disseminated intravascular coagulation

Author(s):  
Mamta Sharma ◽  
Rajkumar .

Disseminated intravascular coagulation is a life threatening complication of ectopic pregnancy. It results from washing out of all important procoagulants. This is basically a state of increased propensity for clot formation triggered by a variety of stimuli related to such diverse disorders as sepsis ,endothelial cell damage (heat stroke and shock), obstetrical complication (abruptio placenta, amniotic fluid embolism, severe preeclampsia and retained intrauterine dead foetus). A case of disseminated intravascular coagulation with septicemic shock following laprotomy for ectopic pregnancy is reported. She was treated by vasopressors, broad spectrum antibiotic and aggressive blood and blood component therapy.

1970 ◽  
Vol 20 (1) ◽  
pp. 68-74 ◽  
Author(s):  
S Sultana ◽  
A Begum ◽  
MA Khan

Disseminated intravascular coagulation (DIC) is an acquired and complex disorder that occurs in a wide variety of clinical conditions. This is basically a state of increased propensity for clot formation triggered by a variety of stimuli related to such diverse disorders as sepsis, endothelial cell damage (heat stroke, shock), obstetrical complication (abruptio placenta, amniotic fluid embolism, severe preeclampsia and retained intrauterine dead foetus) and neoplasm. DIC is a classic complication of obstetric conditions occurring in more than 50 percent of patients with obstetric causes. In DIC, an unregulated thrombin explosion cause release of free thrombin into the circulation that leads to the clinical features of DIC, with thrombin and plasmin responsible for the thrombotic and haemorrhagic manifestations, respectively. The diagnosis and treatment of this syndrome require an understanding of its pathophysiology, awareness of the disorders that can trigger it and its early recognition. Acute DIC is usually associated with infections, the commonest cause, about 10-20% of patients with gram negative sepsis have evidence of DIC. Chronic DIC is usually associated with retained dead fetus, carcinomatosis. The diagnosis of this syndrome is essentially clinical, with laboratory tests providing confirmatory evidence. Microvascular thrombosis is the primary mechanism in most cases, and end organ failure is a major cause of death. No single diagnostic test exists for DIC. DIC is initially suggested by the following combination; a clinical condition consistent with DIC, thrombocytopenia, prolonged PT, APTT, and presence of FDP/D-dimer. Medical treatment depends on the cause of the DIC. Basically it involves removing the cause for example, delivery of placenta if it is retained or abrupted, delivery of foetus if retained, quick delivery if severe eclampsia and so on, hysterectomy if bleeding can not be controlled from placental site. After then, and/or con-currently treat DIC with blood and plasma transfusions and appropriate supportive measures. As the sequel of DIC can be devastating, early clinical suspicion and laboratory diagnosis are essential. This review article provides essential guideline for the appropriate diagnosis and clinical management of DIC in obstetric patients. Key words: Disseminated intravascular coagulation (DIC); Obstetric; Thrombosis; Fibrin; Ddimer; FDP; Anticoagulant. DOI: http://dx.doi.org/10.3329/jdmc.v20i1.8585 J Dhaka Med Coll. 2011; 20(1) :68-74  


2018 ◽  
Vol 2018 ◽  
pp. 1-3
Author(s):  
Uroosa Ibrahim ◽  
Amina Saqib ◽  
Maryam Rehan ◽  
Jean Paul Atallah

Hemophagocytic lymphohistiocytosis (HLH) is a life-threatening disorder that can be familial in etiology or a result of infections, malignancy, and autoimmune or inflammatory disorders. Disseminated intravascular coagulation (DIC) is common in patients admitted to intensive care units and can confound and delay the diagnosis of HLH. We present a case of a 69-year-old female who presented with dyspnea and malaise. Her condition declined rapidly with laboratory parameters consistent with DIC. In addition, she had a ferritin of 32,522 ng/mL, low haptoglobin, and elevated LDH, and bone marrow biopsy showed hemophagocytic lymphohistiocytes. She was started on HLH-directed therapy, and later, a diagnosis of ALK-negative anaplastic large cell lymphoma was made on an excisional inguinal lymph node biopsy specimen. Our case emphasizes the importance of prompt recognition, diagnosis, and treatment of HLH while workup for a primary disorder is still being pursued.


1997 ◽  
Vol 15 (3) ◽  
pp. 1272-1282 ◽  
Author(s):  
A A Ashour ◽  
C F Verschraegen ◽  
A P Kudelka ◽  
J J Kavanagh

PURPOSE AND DESIGN The purpose of this review is to define and describe the paraneoplastic syndromes associated with gynecologic neoplasms. A comprehensive search of MEDLINE from 1966 to January 1996 and Cancerlit was performed. One hundred twenty-two reports were reviewed. RESULTS Twenty-four paraneoplastic syndromes have been associated with gynecologic malignancies. Six anatomic systems are affected by these syndromes. However, except for disseminated intravascular coagulation and hypercalcemia, these syndromes are rare. CONCLUSION Paraneoplastic syndromes are not frequently associated with gynecologic malignancies. The diagnosis of these syndromes is essential, as they can be occasionally life-threatening. Some paraneoplastic syndromes can be used as marker of progression or regression of the underlying malignancy.


2019 ◽  
Vol 32 (1) ◽  
pp. 78
Author(s):  
Andreia Sofia Costa ◽  
Anusca Paixão ◽  
Henrique Santos ◽  
Fernando Salvador

Hemophagocytic lymphohistiocytosis is a rare, aggressive and life-threatening syndrome, characterized by an excessive immune activation. It is triggered by multiple stimuli, with infections having an important role. The most common infectious trigger is viral infection, particularly by Epstein-Barr virus. Coagulation disorders are common in hemophagocytic lymphohistiocytosis and disseminated intravascular coagulation can be present in severe cases. We report a clinical case of Epstein-Barr virus-associated hemophagocytic lymphohistiocytosis, complicated with disseminated intravascular coagulation which evolved favorably with only supportive therapy and without specific treatment.


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